CS248025B2 - Production method of new cefemderivatives - Google Patents

Production method of new cefemderivatives

Info

Publication number: CS248025B2
Authority: CS; Czechoslovakia
Prior art keywords: group; carbon atoms; formula; alkyl; substituted
Prior art date: 1981-05-12

Application number

CS823386A

Other languages

Czech (cs)

English (en)

Inventor

Rudolf Lattrell

Manfred Wieduwilt

Walter Duerckheimer

Juergen Blumbach

Karl Seeger

Original Assignee

Hoechst Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1981-05-12

Filing date

1982-05-10

Publication date

1987-01-15

1982-05-10 Application filed by Hoechst Ag filed Critical Hoechst Ag

1987-01-15 Publication of CS248025B2 publication Critical patent/CS248025B2/cs

Links

238000004519 manufacturing process Methods 0.000 title claims 2
-1 C 1 -C 6 alkyloxy Chemical group 0.000 claims description 138
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 87
150000001875 compounds Chemical class 0.000 claims description 64
125000004432 carbon atom Chemical group C* 0.000 claims description 49
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 40
239000002253 acid Substances 0.000 claims description 35
125000000217 alkyl group Chemical group 0.000 claims description 29
FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims description 24
125000001424 substituent group Chemical group 0.000 claims description 21
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 18
150000003839 salts Chemical class 0.000 claims description 17
238000000034 method Methods 0.000 claims description 16
229910052739 hydrogen Inorganic materials 0.000 claims description 14
229910052760 oxygen Inorganic materials 0.000 claims description 14
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 12
101100073357 Streptomyces halstedii sch2 gene Proteins 0.000 claims description 11
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 11
229910052736 halogen Inorganic materials 0.000 claims description 11
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 10
150000002367 halogens Chemical class 0.000 claims description 10
239000001257 hydrogen Substances 0.000 claims description 10
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
125000003545 alkoxy group Chemical group 0.000 claims description 9
229910052799 carbon Inorganic materials 0.000 claims description 9
229910052757 nitrogen Inorganic materials 0.000 claims description 9
125000006239 protecting group Chemical group 0.000 claims description 9
150000003222 pyridines Chemical class 0.000 claims description 9
229910052717 sulfur Inorganic materials 0.000 claims description 9
125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 8
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 claims description 5
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 5
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 5
150000001782 cephems Chemical class 0.000 claims description 5
125000000753 cycloalkyl group Chemical group 0.000 claims description 5
125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
239000011593 sulfur Substances 0.000 claims description 5
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 4
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 4
125000003342 alkenyl group Chemical group 0.000 claims description 4
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 4
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 4
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 4
230000000269 nucleophilic effect Effects 0.000 claims description 4
239000001301 oxygen Substances 0.000 claims description 4
125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims description 3
125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 3
125000003806 alkyl carbonyl amino group Chemical group 0.000 claims description 3
150000001721 carbon Chemical group 0.000 claims description 3
125000000392 cycloalkenyl group Chemical group 0.000 claims description 3
125000005843 halogen group Chemical group 0.000 claims description 3
230000007935 neutral effect Effects 0.000 claims description 3
125000004043 oxo group Chemical group O=* 0.000 claims description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 2
125000003302 alkenyloxy group Chemical group 0.000 claims description 2
125000000304 alkynyl group Chemical group 0.000 claims description 2
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 2
125000004093 cyano group Chemical group *C#N 0.000 claims description 2
125000004981 cycloalkylmethyl group Chemical group 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 2
ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims description 2
125000004076 pyridyl group Chemical group 0.000 claims description 2
239000007858 starting material Substances 0.000 claims description 2
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 2
125000001544 thienyl group Chemical group 0.000 claims description 2
125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 1
QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical group ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 claims 1
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 78
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 39
150000003951 lactams Chemical group 0.000 description 28
239000000203 mixture Substances 0.000 description 26
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 24
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 22
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 21
238000006243 chemical reaction Methods 0.000 description 21
238000007792 addition Methods 0.000 description 20
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 19
238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 18
239000007787 solid Substances 0.000 description 17
DTQVDTLACAAQTR-DYCDLGHISA-N trifluoroacetic acid-d1 Chemical compound [2H]OC(=O)C(F)(F)F DTQVDTLACAAQTR-DYCDLGHISA-N 0.000 description 17
125000001309 chloro group Chemical group Cl* 0.000 description 14
LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 14
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 13
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
239000000047 product Substances 0.000 description 12
239000000243 solution Substances 0.000 description 11
VJXRKZJMGVSXPX-UHFFFAOYSA-N 4-ethylpyridine Chemical compound CCC1=CC=NC=C1 VJXRKZJMGVSXPX-UHFFFAOYSA-N 0.000 description 10
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 10
WLQVBFDHWAVUJN-UHFFFAOYSA-N 4-cyclopropylpyridine Chemical compound C1CC1C1=CC=NC=C1 WLQVBFDHWAVUJN-UHFFFAOYSA-N 0.000 description 9
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 9
239000000741 silica gel Substances 0.000 description 9
229910002027 silica gel Inorganic materials 0.000 description 9
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 8
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 8
RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 8
150000003254 radicals Chemical class 0.000 description 8
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 7
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical group CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 6
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
239000000460 chlorine Substances 0.000 description 6
239000012043 crude product Substances 0.000 description 6
239000011541 reaction mixture Substances 0.000 description 6
FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 6
MGADZUXDNSDTHW-UHFFFAOYSA-N 2H-pyran Chemical compound C1OC=CC=C1 MGADZUXDNSDTHW-UHFFFAOYSA-N 0.000 description 5
235000011054 acetic acid Nutrition 0.000 description 5
125000001246 bromo group Chemical group Br* 0.000 description 5
150000001732 carboxylic acid derivatives Chemical class 0.000 description 5
230000035622 drinking Effects 0.000 description 5
239000003480 eluent Substances 0.000 description 5
238000002329 infrared spectrum Methods 0.000 description 5
239000002244 precipitate Substances 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 5
QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 4
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 4
UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
150000007513 acids Chemical class 0.000 description 4
239000004480 active ingredient Substances 0.000 description 4
150000001408 amides Chemical class 0.000 description 4
125000003277 amino group Chemical group 0.000 description 4
150000008064 anhydrides Chemical class 0.000 description 4
150000001735 carboxylic acids Chemical class 0.000 description 4
238000001816 cooling Methods 0.000 description 4
125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 4
238000004108 freeze drying Methods 0.000 description 4
239000002904 solvent Substances 0.000 description 4
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
229930186147 Cephalosporin Natural products 0.000 description 3
101150065749 Churc1 gene Proteins 0.000 description 3
241000543381 Cliftonia monophylla Species 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 3
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 3
102100038239 Protein Churchill Human genes 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 3
229910000147 aluminium phosphate Inorganic materials 0.000 description 3
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
229940124587 cephalosporin Drugs 0.000 description 3
150000001780 cephalosporins Chemical class 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
125000002668 chloroacetyl group Chemical group ClCC(=O)* 0.000 description 3
239000003085 diluting agent Substances 0.000 description 3
239000003814 drug Substances 0.000 description 3
238000001035 drying Methods 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000000706 filtrate Substances 0.000 description 3
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
125000004430 oxygen atom Chemical group O* 0.000 description 3
235000015497 potassium bicarbonate Nutrition 0.000 description 3
229910000028 potassium bicarbonate Inorganic materials 0.000 description 3
239000011736 potassium bicarbonate Substances 0.000 description 3
TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 3
JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 3
229910000030 sodium bicarbonate Inorganic materials 0.000 description 3
235000017557 sodium bicarbonate Nutrition 0.000 description 3
238000003756 stirring Methods 0.000 description 3
125000004434 sulfur atom Chemical group 0.000 description 3
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
ASOKPJOREAFHNY-UHFFFAOYSA-N 1-Hydroxybenzotriazole Chemical compound C1=CC=C2N(O)N=NC2=C1 ASOKPJOREAFHNY-UHFFFAOYSA-N 0.000 description 2
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 2
YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 2
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
241000894006 Bacteria Species 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 2
241000735552 Erythroxylum Species 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
101000986989 Naja kaouthia Acidic phospholipase A2 CM-II Proteins 0.000 description 2
GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
101100054666 Streptomyces halstedii sch3 gene Proteins 0.000 description 2
125000004448 alkyl carbonyl group Chemical group 0.000 description 2
RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
230000000844 anti-bacterial effect Effects 0.000 description 2
125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 2
239000002775 capsule Substances 0.000 description 2
YGBFLZPYDUKSPT-MRVPVSSYSA-N cephalosporanic acid Chemical compound S1CC(COC(=O)C)=C(C(O)=O)N2C(=O)C[C@H]21 YGBFLZPYDUKSPT-MRVPVSSYSA-N 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
238000003776 cleavage reaction Methods 0.000 description 2
ZXFCRFYULUUSDW-LANRQRAVSA-N cmt-3 Chemical compound C1C2CC3=CC=CC(O)=C3C(=O)C2=C(O)[C@@]2(O)C1CC(O)=C(C(=O)N)C2=O ZXFCRFYULUUSDW-LANRQRAVSA-N 0.000 description 2
235000008957 cocaer Nutrition 0.000 description 2
ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 description 2
MLIREBYILWEBDM-UHFFFAOYSA-N cyanoacetic acid Chemical compound OC(=O)CC#N MLIREBYILWEBDM-UHFFFAOYSA-N 0.000 description 2
125000004966 cyanoalkyl group Chemical group 0.000 description 2
125000004122 cyclic group Chemical group 0.000 description 2
125000001162 cycloheptenyl group Chemical group C1(=CCCCCC1)* 0.000 description 2
HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
125000004185 ester group Chemical group 0.000 description 2
125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 2
230000002349 favourable effect Effects 0.000 description 2
125000001153 fluoro group Chemical group F* 0.000 description 2
150000004820 halides Chemical class 0.000 description 2
125000005842 heteroatom Chemical group 0.000 description 2
150000002431 hydrogen Chemical class 0.000 description 2
238000011065 in-situ storage Methods 0.000 description 2
239000012442 inert solvent Substances 0.000 description 2
208000015181 infectious disease Diseases 0.000 description 2
239000000463 material Substances 0.000 description 2
229940098779 methanesulfonic acid Drugs 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
230000000813 microbial effect Effects 0.000 description 2
229910017604 nitric acid Inorganic materials 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
239000012074 organic phase Substances 0.000 description 2
CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 2
239000000546 pharmaceutical excipient Substances 0.000 description 2
UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 description 2
TURAMGVWNUTQKH-UHFFFAOYSA-N propa-1,2-dien-1-one Chemical group C=C=C=O TURAMGVWNUTQKH-UHFFFAOYSA-N 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
230000035484 reaction time Effects 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
230000007017 scission Effects 0.000 description 2
XGVXKJKTISMIOW-ZDUSSCGKSA-N simurosertib Chemical compound N1N=CC(C=2SC=3C(=O)NC(=NC=3C=2)[C@H]2N3CCC(CC3)C2)=C1C XGVXKJKTISMIOW-ZDUSSCGKSA-N 0.000 description 2
239000011734 sodium Substances 0.000 description 2
235000009518 sodium iodide Nutrition 0.000 description 2
239000011877 solvent mixture Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
DYHSDKLCOJIUFX-UHFFFAOYSA-N tert-butoxycarbonyl anhydride Chemical compound CC(C)(C)OC(=O)OC(=O)OC(C)(C)C DYHSDKLCOJIUFX-UHFFFAOYSA-N 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
QBUMXSSCYUMVAW-UHFFFAOYSA-N 1-bromocyclohexene Chemical group BrC1=CCCCC1 QBUMXSSCYUMVAW-UHFFFAOYSA-N 0.000 description 1
NDVMCQUOSYOQMZ-UHFFFAOYSA-N 2,2-bis(trimethylsilyl)acetamide Chemical compound C[Si](C)(C)C(C(N)=O)[Si](C)(C)C NDVMCQUOSYOQMZ-UHFFFAOYSA-N 0.000 description 1
JKTCBAGSMQIFNL-UHFFFAOYSA-N 2,3-dihydrofuran Chemical compound C1CC=CO1 JKTCBAGSMQIFNL-UHFFFAOYSA-N 0.000 description 1
UFBJCMHMOXMLKC-UHFFFAOYSA-N 2,4-dinitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O UFBJCMHMOXMLKC-UHFFFAOYSA-N 0.000 description 1
FUJSJWRORKKPAI-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)acetyl chloride Chemical compound ClC(=O)COC1=CC=C(Cl)C=C1Cl FUJSJWRORKKPAI-UHFFFAOYSA-N 0.000 description 1
125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 1
CFMZSMGAMPBRBE-UHFFFAOYSA-N 2-hydroxyisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(O)C(=O)C2=C1 CFMZSMGAMPBRBE-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
PXFXRVCGZAGBRR-UHFFFAOYSA-N 3,4-dihydro-2h-pyrano[3,2-c]pyridine Chemical compound C1=NC=C2CCCOC2=C1 PXFXRVCGZAGBRR-UHFFFAOYSA-N 0.000 description 1
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
ITQTTZVARXURQS-UHFFFAOYSA-N 3-methylpyridine Chemical compound CC1=CC=CN=C1 ITQTTZVARXURQS-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 description 1
FKNQCJSGGFJEIZ-UHFFFAOYSA-N 4-methylpyridine Chemical compound CC1=CC=NC=C1 FKNQCJSGGFJEIZ-UHFFFAOYSA-N 0.000 description 1
BTJIUGUIPKRLHP-UHFFFAOYSA-N 4-nitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1 BTJIUGUIPKRLHP-UHFFFAOYSA-N 0.000 description 1
XFDCNXIWKCIBAE-UHFFFAOYSA-N 5-bromo-1,3-thiazol-2-amine;hydrochloride Chemical compound Cl.NC1=NC=C(Br)S1 XFDCNXIWKCIBAE-UHFFFAOYSA-N 0.000 description 1
HSHGZXNAXBPPDL-HZGVNTEJSA-N 7beta-aminocephalosporanic acid Chemical compound S1CC(COC(=O)C)=C(C([O-])=O)N2C(=O)[C@@H]([NH3+])[C@@H]12 HSHGZXNAXBPPDL-HZGVNTEJSA-N 0.000 description 1
229920001817 Agar Polymers 0.000 description 1
241000416162 Astragalus gummifer Species 0.000 description 1
108020004256 Beta-lactamase Proteins 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
UIOAQJNADLELPQ-UHFFFAOYSA-N C[C]1OCCO1 Chemical group C[C]1OCCO1 UIOAQJNADLELPQ-UHFFFAOYSA-N 0.000 description 1
NMEZJSDUZQOPFE-UHFFFAOYSA-N Cyclohex-1-enecarboxylic acid Chemical group OC(=O)C1=CCCCC1 NMEZJSDUZQOPFE-UHFFFAOYSA-N 0.000 description 1
BUDQDWGNQVEFAC-UHFFFAOYSA-N Dihydropyran Chemical compound C1COC=CC1 BUDQDWGNQVEFAC-UHFFFAOYSA-N 0.000 description 1
241000206672 Gelidium Species 0.000 description 1
101000713585 Homo sapiens Tubulin beta-4A chain Proteins 0.000 description 1
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 1
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
NQTADLQHYWFPDB-UHFFFAOYSA-N N-Hydroxysuccinimide Chemical compound ON1C(=O)CCC1=O NQTADLQHYWFPDB-UHFFFAOYSA-N 0.000 description 1
229930182555 Penicillin Natural products 0.000 description 1
108010087702 Penicillinase Proteins 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
101100334474 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) NOP1 gene Proteins 0.000 description 1
PLGPSDNOLCVGSS-UHFFFAOYSA-N Tetraphenylcyclopentadienone Chemical compound O=C1C(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)C(C=2C=CC=CC=2)=C1C1=CC=CC=C1 PLGPSDNOLCVGSS-UHFFFAOYSA-N 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
229920001615 Tragacanth Polymers 0.000 description 1
102100036788 Tubulin beta-4A chain Human genes 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
125000000218 acetic acid group Chemical class C(C)(=O)* 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
230000004913 activation Effects 0.000 description 1
230000010933 acylation Effects 0.000 description 1
238000005917 acylation reaction Methods 0.000 description 1
125000004423 acyloxy group Chemical group 0.000 description 1
235000010419 agar Nutrition 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000004183 alkoxy alkyl group Chemical group 0.000 description 1
125000004687 alkyl sulfinyl alkyl group Chemical group 0.000 description 1
125000004644 alkyl sulfinyl group Chemical group 0.000 description 1
125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
125000006350 alkyl thio alkyl group Chemical group 0.000 description 1
125000004414 alkyl thio group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
125000005133 alkynyloxy group Chemical group 0.000 description 1
125000005336 allyloxy group Chemical group 0.000 description 1
238000007112 amidation reaction Methods 0.000 description 1
229940126575 aminoglycoside Drugs 0.000 description 1
230000000845 anti-microbial effect Effects 0.000 description 1
239000002246 antineoplastic agent Substances 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
150000001540 azides Chemical class 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
SIOVKLKJSOKLIF-UHFFFAOYSA-N bis(trimethylsilyl)acetamide Chemical compound C[Si](C)(C)OC(C)=N[Si](C)(C)C SIOVKLKJSOKLIF-UHFFFAOYSA-N 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
239000000872 buffer Substances 0.000 description 1
125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
125000005242 carbamoyl alkyl group Chemical group 0.000 description 1
150000001718 carbodiimides Chemical class 0.000 description 1
125000004181 carboxyalkyl group Chemical group 0.000 description 1
125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
PODDMJATAWBBPI-UHFFFAOYSA-N chlorosilyl(trimethyl)silane Chemical compound C[Si](C)(C)[SiH2]Cl PODDMJATAWBBPI-UHFFFAOYSA-N 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
239000003086 colorant Substances 0.000 description 1
125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
NIRMDYUESATWJX-UHFFFAOYSA-N cycloheptene-1-carboxamide Chemical group NC(=O)C1=CCCCCC1 NIRMDYUESATWJX-UHFFFAOYSA-N 0.000 description 1
FNFJZXAWCAEGNI-UHFFFAOYSA-N cycloheptene-1-carboxylic acid Chemical group OC(=O)C1=CCCCCC1 FNFJZXAWCAEGNI-UHFFFAOYSA-N 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical group OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
QBJOHGAEIAUULA-UHFFFAOYSA-N cyclohexen-1-ylmethanol Chemical group OCC1=CCCCC1 QBJOHGAEIAUULA-UHFFFAOYSA-N 0.000 description 1
SNDQOBHHPNQOBB-UHFFFAOYSA-N cyclohexene-1-carboxamide Chemical group NC(=O)C1=CCCCC1 SNDQOBHHPNQOBB-UHFFFAOYSA-N 0.000 description 1
125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 1
125000004145 cyclopenten-1-yl group Chemical group [H]C1=C(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
125000004851 cyclopentylmethyl group Chemical group C1(CCCC1)C* 0.000 description 1
229940127089 cytotoxic agent Drugs 0.000 description 1
238000010908 decantation Methods 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
229940113088 dimethylacetamide Drugs 0.000 description 1
239000008298 dragée Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000004494 ethyl ester group Chemical group 0.000 description 1
125000006351 ethylthiomethyl group Chemical group [H]C([H])([H])C([H])([H])SC([H])([H])* 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000000796 flavoring agent Substances 0.000 description 1
235000013355 food flavoring agent Nutrition 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
125000004005 formimidoyl group Chemical group [H]\N=C(/[H])* 0.000 description 1
239000000499 gel Substances 0.000 description 1
230000002140 halogenating effect Effects 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
239000005457 ice water Substances 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
239000002198 insoluble material Substances 0.000 description 1
239000013067 intermediate product Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
150000002596 lactones Chemical class 0.000 description 1
239000008101 lactose Substances 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
125000005394 methallyl group Chemical group 0.000 description 1
UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
VTYCAXIAUKEGBQ-UHFFFAOYSA-N methyl cyclopentene-1-carboxylate Chemical group COC(=O)C1=CCCC1 VTYCAXIAUKEGBQ-UHFFFAOYSA-N 0.000 description 1
125000004372 methylthioethyl group Chemical group [H]C([H])([H])SC([H])([H])C([H])([H])* 0.000 description 1
125000004092 methylthiomethyl group Chemical group [H]C([H])([H])SC([H])([H])* 0.000 description 1
238000002156 mixing Methods 0.000 description 1
PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
238000007911 parenteral administration Methods 0.000 description 1
229950009506 penicillinase Drugs 0.000 description 1
150000002960 penicillins Chemical class 0.000 description 1
239000008194 pharmaceutical composition Substances 0.000 description 1
230000000144 pharmacologic effect Effects 0.000 description 1
IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
235000011181 potassium carbonates Nutrition 0.000 description 1
229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
229940116357 potassium thiocyanate Drugs 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
125000004964 sulfoalkyl group Chemical group 0.000 description 1
239000003826 tablet Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
230000002110 toxicologic effect Effects 0.000 description 1
231100000027 toxicology Toxicity 0.000 description 1
239000000196 tragacanth Substances 0.000 description 1
235000010487 tragacanth Nutrition 0.000 description 1
229940116362 tragacanth Drugs 0.000 description 1
125000004665 trialkylsilyl group Chemical group 0.000 description 1
YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 description 1
239000003039 volatile agent Substances 0.000 description 1
238000005303 weighing Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
- C07D501/14—Compounds having a nitrogen atom directly attached in position 7
- C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
- C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
- C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
- C07D501/38—Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof
- C07D501/46—Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof with the 7-amino radical acylated by carboxylic acids containing hetero rings
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Life Sciences & Earth Sciences (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Communicable Diseases (AREA)
Pharmacology & Pharmacy (AREA)
Oncology (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Cephalosporin Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

CS823386A 1981-05-12 1982-05-10 Production method of new cefemderivatives CS248025B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19813118732 DE3118732A1 (de)	1981-05-12	1981-05-12	Cephalosporinderivate und verfahren zu ihrer herstellung

Publications (1)

Publication Number	Publication Date
CS248025B2 true CS248025B2 (en)	1987-01-15

Family

ID=6132055

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
CS823386A CS248025B2 (en)	1981-05-12	1982-05-10	Production method of new cefemderivatives
CS914158A CS415891A3 (en)	1981-05-12	1991-12-30	Cephalosporin derivatives and process for preparing thereof

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
CS914158A CS415891A3 (en)	1981-05-12	1991-12-30	Cephalosporin derivatives and process for preparing thereof

Country Status (36)

Country	Link
US (1)	US5071979A (pt)
EP (1)	EP0064740B1 (pt)
JP (2)	JPS57192394A (pt)
KR (1)	KR880001541B1 (pt)
AR (1)	AR241186A1 (pt)
AT (2)	ATE19085T1 (pt)
AU (1)	AU559727B2 (pt)
BE (1)	BE893163A (pt)
BG (1)	BG60838B2 (pt)
CA (1)	CA1228850A (pt)
CH (1)	CH654312A5 (pt)
CS (2)	CS248025B2 (pt)
DD (1)	DD202720A5 (pt)
DE (2)	DE3118732A1 (pt)
DK (1)	DK166500B1 (pt)
DZ (1)	DZ418A1 (pt)
ES (1)	ES511955A0 (pt)
FI (1)	FI70715C (pt)
FR (2)	FR2511682B1 (pt)
GB (2)	GB2098216A (pt)
GR (1)	GR75506B (pt)
HU (1)	HU186019B (pt)
IE (1)	IE53296B1 (pt)
IL (1)	IL65737A (pt)
IT (1)	IT1157275B (pt)
LU (1)	LU88736I2 (pt)
MA (1)	MA19474A1 (pt)
MT (1)	MTP909B (pt)
NL (3)	NL8201913A (pt)
NO (2)	NO162022C (pt)
NZ (1)	NZ200567A (pt)
PH (1)	PH20243A (pt)
PT (1)	PT74877B (pt)
SE (1)	SE8202961L (pt)
YU (1)	YU44346B (pt)
ZA (1)	ZA823226B (pt)

Families Citing this family (54)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3118732A1 (de) *	1981-05-12	1982-12-02	Hoechst Ag, 6000 Frankfurt	Cephalosporinderivate und verfahren zu ihrer herstellung
GR76701B (pt) *	1981-09-08	1984-08-29	Lilly Co Eli
JPS5859991A (ja) *	1981-09-14	1983-04-09	Fujisawa Pharmaceut Co Ltd	新規セフェム化合物
US4501739A (en) *	1982-01-19	1985-02-26	Eli Lilly And Company	Thieno and furopyridinium-substituted cephalosporins
DE3207840A1 (de) *	1982-03-04	1983-09-15	Hoechst Ag, 6230 Frankfurt	"cephalosporinderivate und verfahren zu ihrer herstellung"
EP0097961B1 (en) *	1982-06-28	1987-11-11	Bristol-Myers Company	Cephalosporin derivatives, a process for the manufacture thereof and pharmaceutical compositions containing said derivatives
DE3247613A1 (de) *	1982-12-23	1984-07-05	Hoechst Ag, 6230 Frankfurt	Cephalosporinderivate und verfahren zu ihrer herstellung
DE3248281A1 (de) *	1982-12-28	1984-06-28	Hoechst Ag, 6230 Frankfurt	Kristalisierte cephem-saeureadditionssalze und verfahren zu ihrer herstellung
DE3316798A1 (de) *	1983-05-07	1984-11-08	Hoechst Ag, 6230 Frankfurt	Verfahren zur herstellung von cephemverbindungen
DE3316797A1 (de) *	1983-05-07	1984-11-08	Hoechst Ag, 6230 Frankfurt	Verfahren zur herstellung von cephemverbindungen
US4690921A (en) *	1983-10-11	1987-09-01	Yamanouchi Pharmaceutical Co., Ltd.	Cephalosporin compounds and salts thereof
ZA847926B (en) *	1983-10-17	1986-05-28	Lilly Co Eli	3-bicyclicpyridinium-methyl cephalosporins
US4692443A (en) *	1983-10-17	1987-09-08	Eli Lilly And Company	3-bicyclicpyridinium-methyl cephalosporins
JPS6094984A (ja) *	1983-10-28	1985-05-28	Dai Ichi Seiyaku Co Ltd	セフエム誘導体
GB8401093D0 (en) *	1984-01-16	1984-02-15	Fujisawa Pharmaceutical Co	Cephem compounds
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1981
- 1981-05-12 DE DE19813118732 patent/DE3118732A1/de not_active Withdrawn
1982
- 1982-05-06 ES ES511955A patent/ES511955A0/es active Granted
- 1982-05-07 AR AR82289339A patent/AR241186A1/es active
- 1982-05-07 LU LU88736C patent/LU88736I2/fr unknown
- 1982-05-07 EP EP82103989A patent/EP0064740B1/de not_active Expired
- 1982-05-07 AT AT82103989T patent/ATE19085T1/de active
- 1982-05-07 DE DE8282103989T patent/DE3270360D1/de not_active Expired
- 1982-05-10 IT IT21182/82A patent/IT1157275B/it active
- 1982-05-10 MT MT909A patent/MTP909B/xx unknown
- 1982-05-10 DD DD82239724A patent/DD202720A5/de not_active IP Right Cessation
- 1982-05-10 PH PH27254A patent/PH20243A/en unknown
- 1982-05-10 CS CS823386A patent/CS248025B2/cs unknown
- 1982-05-10 FR FR8208066A patent/FR2511682B1/fr not_active Expired
- 1982-05-10 KR KR8202031A patent/KR880001541B1/ko active
- 1982-05-10 US US06/376,654 patent/US5071979A/en not_active Expired - Lifetime
- 1982-05-10 FI FI821644A patent/FI70715C/fi not_active IP Right Cessation
- 1982-05-10 NL NL8201913A patent/NL8201913A/nl not_active Application Discontinuation
- 1982-05-10 NZ NZ200567A patent/NZ200567A/en unknown
- 1982-05-10 CH CH2899/82A patent/CH654312A5/de not_active IP Right Cessation
- 1982-05-10 YU YU983/82A patent/YU44346B/xx unknown
- 1982-05-10 JP JP57078063A patent/JPS57192394A/ja active Granted
- 1982-05-10 GR GR68118A patent/GR75506B/el unknown
- 1982-05-11 DK DK211382A patent/DK166500B1/da not_active IP Right Cessation
- 1982-05-11 IL IL65737A patent/IL65737A/xx not_active IP Right Cessation
- 1982-05-11 ZA ZA823226A patent/ZA823226B/xx unknown
- 1982-05-11 AU AU83589/82A patent/AU559727B2/en not_active Expired
- 1982-05-11 PT PT74877A patent/PT74877B/pt unknown
- 1982-05-11 NO NO821562A patent/NO162022C/no not_active IP Right Cessation
- 1982-05-11 SE SE8202961A patent/SE8202961L/ not_active Application Discontinuation
- 1982-05-11 HU HU821467A patent/HU186019B/hu unknown
- 1982-05-11 IE IE1129/82A patent/IE53296B1/en not_active IP Right Cessation
- 1982-05-11 AT AT0184382A patent/AT381945B/de not_active IP Right Cessation
- 1982-05-11 CA CA000402656A patent/CA1228850A/en not_active Expired
- 1982-05-12 MA MA19680A patent/MA19474A1/fr unknown
- 1982-05-12 GB GB8213782A patent/GB2098216A/en not_active Revoked
- 1982-05-12 BE BE0/208075A patent/BE893163A/fr not_active IP Right Cessation
- 1982-05-12 DZ DZ826531A patent/DZ418A1/fr active
- 1982-12-13 FR FR8220875A patent/FR2515654B1/fr not_active Expired
1984
- 1984-09-18 GB GB08423511A patent/GB2144424B/en not_active Expired
1987
- 1987-12-28 JP JP62336812A patent/JPH0670068B2/ja not_active Expired - Lifetime
1991
- 1991-12-30 CS CS914158A patent/CS415891A3/cs unknown
1994
- 1994-02-22 NL NL940003C patent/NL940003I2/nl unknown
- 1994-02-24 BG BG098550A patent/BG60838B2/bg unknown
1995
- 1995-08-08 NL NL950013C patent/NL950013I1/nl unknown
1999
- 1999-05-27 NO NO1999008C patent/NO1999008I1/no unknown

Also Published As

Publication number	Publication date
HU186019B (en)	1985-05-28
US5071979A (en)	1991-12-10
NO162022C (no)	1989-10-25
BG60838B2 (bg)	1996-04-30
DE3270360D1 (en)	1986-05-15
GB2098216A (en)	1982-11-17
NZ200567A (en)	1985-01-31
MTP909B (en)	1985-02-28
AR241186A1 (es)	1992-01-31
NO1999008I1 (no)	1999-05-27
FR2511682B1 (fr)	1985-06-28
DE3118732A1 (de)	1982-12-02
ZA823226B (en)	1983-03-30
JPS57192394A (en)	1982-11-26
EP0064740A2 (de)	1982-11-17
DK166500B1 (da)	1993-06-01
DZ418A1 (fr)	2004-09-13
SE8202961L (sv)	1982-11-13
NL950013I2 (nl)	1997-02-03
AU559727B2 (en)	1987-03-19
YU44346B (en)	1990-06-30
NO821562L (no)	1982-11-15
ATE19085T1 (de)	1986-04-15
AT381945B (de)	1986-12-10
JPS6419082A (en)	1989-01-23
FI821644L (fi)	1982-11-13
PT74877A (de)	1982-06-01
FR2515654A1 (fr)	1983-05-06
IT1157275B (it)	1987-02-11
DD202720A5 (de)	1983-09-28
IE821129L (en)	1982-11-12
EP0064740B1 (de)	1986-04-09
SE8202961D0 (sv)	1982-05-11
ATA184382A (de)	1986-05-15
IL65737A (en)	1986-11-30
FR2511682A1 (fr)	1983-02-25
GB2144424A (en)	1985-03-06
IE53296B1 (en)	1988-10-12
BE893163A (fr)	1982-11-12
NL950013I1 (nl)	1997-02-03
AU8358982A (en)	1982-11-18
LU88736I2 (fr)	1996-08-23
MA19474A1 (fr)	1982-12-31
KR830010121A (ko)	1983-12-26
CS415891A3 (en)	1992-04-15
FI70715C (fi)	1986-10-06
CH654312A5 (de)	1986-02-14
GB8423511D0 (en)	1984-10-24
GB2144424B (en)	1986-02-12
FR2515654B1 (fr)	1986-11-14
PH20243A (en)	1986-11-10
NO162022B (no)	1989-07-17
JPH0670068B2 (ja)	1994-09-07
CA1228850A (en)	1987-11-03
DK211382A (da)	1982-11-13
ES8304143A1 (es)	1983-02-16
EP0064740A3 (en)	1983-11-23
JPH0144190B2 (pt)	1989-09-26
IT8221182A0 (it)	1982-05-10
KR880001541B1 (ko)	1988-08-20
ES511955A0 (es)	1983-02-16
IL65737A0 (en)	1982-08-31
FI70715B (fi)	1986-06-26
FI821644A0 (fi)	1982-05-10
YU98382A (en)	1985-08-31
PT74877B (de)	1984-11-26
NL8201913A (nl)	1982-12-01
GR75506B (pt)	1984-07-24
NL940003I2 (nl)	1997-02-03
NL940003I1 (nl)	1994-04-05

Publication	Publication Date	Title
CS248025B2 (en)	1987-01-15	Production method of new cefemderivatives
US4647556A (en)	1987-03-03	Cephalosporin derivatives
JPH0365350B2 (pt)	1991-10-11
US4396619A (en)	1983-08-02	Cephalosporin betaines
US4692443A (en)	1987-09-08	3-bicyclicpyridinium-methyl cephalosporins
EP0397511B1 (en)	1996-09-04	Novel cephalosporin compounds and processes for preparation thereof
US4748172A (en)	1988-05-31	3-bicyclicpyridinium-methyl cephalosporins
EP0267733A2 (en)	1988-05-18	Cephalosporin compounds, process for their preparation and pharmaceutical compositions containing them
CS248714B2 (en)	1987-02-12	Production method of new 7-(2 syn-oxomino-(5 amino-1,2,4-thiadiazol-3-y)cefeme derivatives
CA2131769C (en)	1999-12-28	Novel cephalosporin antibiotics and processes for preparation thereof
HU191911B (en)	1987-04-28	Process for producing intermediate of cephtazidim
DE3330605A1 (de)	1985-03-14	Cephalosporinderivate und verfahren zu ihrer herstellung
EP0453952A2 (en)	1991-10-30	A process for synthesizing cephalosporin compounds
CA2117679C (en)	2000-03-07	Novel cephalosporin antibiotics and processes for the preparation thereof
EP0508375A2 (en)	1992-10-14	Novel cephalosporin compounds and processes for preparation thereof
EP0584797A2 (en)	1994-03-02	Novel cephalosporin compounds and processes for the preparation thereof
JPS6097983A (ja)	1985-05-31	セフアロスポリン誘導体、その製法および医薬組成物
JPH1036375A (ja)	1998-02-10	新規なセファロスポリン誘導体またはその塩
KR100377559B1 (ko)	2003-03-26	경구투여 가능한 세팔로스포린계 화합물 및 이의 제조방법
WO1999058535A1 (en)	1999-11-18	Novel cephalosporin compounds, processes for preparation thereof and antimicrobial compositions containing the same
KR0154901B1 (ko)	1998-11-16	신규 세팔로스포린계 항생제(v)
AU609452B2 (en)	1991-05-02	Cephalosporin derivatives and a process for the preparation thereof
KR930010628B1 (ko)	1993-11-02	신규 세팔로스포린계 항생제 및 그의 제조방법
CA1271741A (en)	1990-07-17	Cephem derivatives
KR910007980B1 (ko)	1991-10-05	신규 세팔로스포린계 항생제 및 이의 제조방법