ZA200209991B - Compounds to treat Alzheimer's disease. - Google Patents
Compounds to treat Alzheimer's disease. Download PDFInfo
- Publication number
- ZA200209991B ZA200209991B ZA200209991A ZA200209991A ZA200209991B ZA 200209991 B ZA200209991 B ZA 200209991B ZA 200209991 A ZA200209991 A ZA 200209991A ZA 200209991 A ZA200209991 A ZA 200209991A ZA 200209991 B ZA200209991 B ZA 200209991B
- Authority
- ZA
- South Africa
- Prior art keywords
- amino
- hydroxy
- dipropylisophthalamide
- propyl
- difluorobenzyl
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims description 90
- 208000024827 Alzheimer disease Diseases 0.000 title claims description 41
- 150000001412 amines Chemical class 0.000 claims abstract description 111
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 31
- 201000010099 disease Diseases 0.000 claims abstract description 26
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2102
- -1 pryidazinyl Chemical group 0.000 claims description 1189
- 125000000217 alkyl group Chemical group 0.000 claims description 219
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 104
- 229910052799 carbon Inorganic materials 0.000 claims description 101
- 125000003545 alkoxy group Chemical group 0.000 claims description 81
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 73
- 125000001424 substituent group Chemical group 0.000 claims description 60
- 229910052739 hydrogen Inorganic materials 0.000 claims description 50
- 125000001072 heteroaryl group Chemical group 0.000 claims description 47
- 125000000623 heterocyclic group Chemical group 0.000 claims description 45
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 41
- 150000001540 azides Chemical class 0.000 claims description 33
- 125000003342 alkenyl group Chemical group 0.000 claims description 29
- 125000000304 alkynyl group Chemical group 0.000 claims description 28
- 108010043324 Amyloid Precursor Protein Secretases Proteins 0.000 claims description 26
- 102000002659 Amyloid Precursor Protein Secretases Human genes 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 22
- 102100022704 Amyloid-beta precursor protein Human genes 0.000 claims description 18
- DZHSAHHDTRWUTF-SIQRNXPUSA-N amyloid-beta polypeptide 42 Chemical compound C([C@@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)NCC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(O)=O)[C@@H](C)CC)C(C)C)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C(C)C)C1=CC=CC=C1 DZHSAHHDTRWUTF-SIQRNXPUSA-N 0.000 claims description 18
- 101710137189 Amyloid-beta A4 protein Proteins 0.000 claims description 17
- 101710151993 Amyloid-beta precursor protein Proteins 0.000 claims description 17
- 238000004519 manufacturing process Methods 0.000 claims description 17
- 229910052757 nitrogen Inorganic materials 0.000 claims description 17
- 108010090849 Amyloid beta-Peptides Proteins 0.000 claims description 13
- 102000013455 Amyloid beta-Peptides Human genes 0.000 claims description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 13
- 206010012289 Dementia Diseases 0.000 claims description 13
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 13
- 150000002118 epoxides Chemical class 0.000 claims description 12
- 210000004556 brain Anatomy 0.000 claims description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
- 239000003814 drug Substances 0.000 claims description 9
- 230000002401 inhibitory effect Effects 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 8
- 238000003776 cleavage reaction Methods 0.000 claims description 8
- 125000004857 imidazopyridinyl group Chemical group N1C(=NC2=C1C=CC=N2)* 0.000 claims description 8
- 230000007017 scission Effects 0.000 claims description 8
- 238000011282 treatment Methods 0.000 claims description 8
- 201000010374 Down Syndrome Diseases 0.000 claims description 7
- 206010044688 Trisomy 21 Diseases 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 7
- 125000004600 benzothiopyranyl group Chemical group S1C(C=CC2=C1C=CC=C2)* 0.000 claims description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- 125000004568 thiomorpholinyl group Chemical group 0.000 claims description 7
- 241001465754 Metazoa Species 0.000 claims description 6
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- 125000003386 piperidinyl group Chemical group 0.000 claims description 6
- 125000002541 furyl group Chemical group 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 125000002757 morpholinyl group Chemical group 0.000 claims description 5
- 125000004193 piperazinyl group Chemical group 0.000 claims description 5
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 5
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 5
- 125000001422 pyrrolinyl group Chemical group 0.000 claims description 5
- 125000005309 thioalkoxy group Chemical group 0.000 claims description 5
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims description 4
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims description 4
- 208000037259 Amyloid Plaque Diseases 0.000 claims description 4
- 150000001408 amides Chemical class 0.000 claims description 4
- 125000002047 benzodioxolyl group Chemical group O1OC(C2=C1C=CC=C2)* 0.000 claims description 4
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims description 4
- 125000004619 benzopyranyl group Chemical group O1C(C=CC2=C1C=CC=C2)* 0.000 claims description 4
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims description 4
- 125000004622 benzoxazinyl group Chemical group O1NC(=CC2=C1C=CC=C2)* 0.000 claims description 4
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims description 4
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims description 4
- 230000002490 cerebral effect Effects 0.000 claims description 4
- 125000003016 chromanyl group Chemical group O1C(CCC2=CC=CC=C12)* 0.000 claims description 4
- 125000004617 chromonyl group Chemical group O1C(=CC(C2=CC=CC=C12)=O)* 0.000 claims description 4
- 125000000259 cinnolinyl group Chemical group N1=NC(=CC2=CC=CC=C12)* 0.000 claims description 4
- 125000000332 coumarinyl group Chemical group O1C(=O)C(=CC2=CC=CC=C12)* 0.000 claims description 4
- 125000005992 dihydrobenzisothiazinyl group Chemical group 0.000 claims description 4
- 125000005993 dihydrobenzisoxazinyl group Chemical group 0.000 claims description 4
- RCCPEORTSYDPMB-UHFFFAOYSA-N hydroxy benzenecarboximidothioate Chemical compound OSC(=N)C1=CC=CC=C1 RCCPEORTSYDPMB-UHFFFAOYSA-N 0.000 claims description 4
- 125000002883 imidazolyl group Chemical group 0.000 claims description 4
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims description 4
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims description 4
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 claims description 4
- 125000003406 indolizinyl group Chemical group C=1(C=CN2C=CC=CC12)* 0.000 claims description 4
- 125000001041 indolyl group Chemical group 0.000 claims description 4
- 125000005994 isobenzotetrahydrofuranyl group Chemical group 0.000 claims description 4
- 125000005990 isobenzothienyl group Chemical group 0.000 claims description 4
- 125000004594 isoindolinyl group Chemical group C1(NCC2=CC=CC=C12)* 0.000 claims description 4
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 claims description 4
- 125000005956 isoquinolyl group Chemical group 0.000 claims description 4
- 125000001786 isothiazolyl group Chemical group 0.000 claims description 4
- 125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 claims description 4
- 125000001715 oxadiazolyl group Chemical group 0.000 claims description 4
- 125000002971 oxazolyl group Chemical group 0.000 claims description 4
- 125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 claims description 4
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 claims description 4
- 125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 claims description 4
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 claims description 4
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 4
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 4
- 125000004076 pyridyl group Chemical group 0.000 claims description 4
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 4
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims description 4
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims description 4
- 125000004620 quinolinyl-N-oxide group Chemical group 0.000 claims description 4
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims description 4
- 125000003039 tetrahydroisoquinolinyl group Chemical group C1(NCCC2=CC=CC=C12)* 0.000 claims description 4
- 125000003831 tetrazolyl group Chemical group 0.000 claims description 4
- 125000001113 thiadiazolyl group Chemical group 0.000 claims description 4
- 125000000335 thiazolyl group Chemical group 0.000 claims description 4
- 125000001544 thienyl group Chemical group 0.000 claims description 4
- 125000004306 triazinyl group Chemical group 0.000 claims description 4
- 125000001425 triazolyl group Chemical group 0.000 claims description 4
- 125000004933 β-carbolinyl group Chemical group C1(=NC=CC=2C3=CC=CC=C3NC12)* 0.000 claims description 4
- 208000032843 Hemorrhage Diseases 0.000 claims description 3
- 241000282412 Homo Species 0.000 claims description 3
- 150000001413 amino acids Chemical class 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 3
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims description 3
- 150000001721 carbon Chemical group 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- 125000005995 isobenzotetrahydrothienyl group Chemical group 0.000 claims description 3
- 125000003384 isochromanyl group Chemical group C1(OCCC2=CC=CC=C12)* 0.000 claims description 3
- 125000003151 isocoumarinyl group Chemical group C1(=O)OC(=CC2=CC=CC=C12)* 0.000 claims description 3
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 3
- 125000001644 phenoxazinyl group Chemical group C1(=CC=CC=2OC3=CC=CC=C3NC12)* 0.000 claims description 3
- 125000005329 tetralinyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 claims description 3
- 230000002792 vascular Effects 0.000 claims description 3
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims description 2
- 150000001204 N-oxides Chemical class 0.000 claims description 2
- 206010002022 amyloidosis Diseases 0.000 claims description 2
- 125000005046 dihydronaphthyl group Chemical group 0.000 claims description 2
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 claims description 2
- 125000006413 ring segment Chemical group 0.000 claims description 2
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 2
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims description 2
- 125000005958 tetrahydrothienyl group Chemical group 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 902
- 125000006497 3-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C(OC([H])([H])[H])=C1[H])C([H])([H])* 0.000 claims 695
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 133
- 125000006482 3-iodobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(I)=C1[H])C([H])([H])* 0.000 claims 126
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 123
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 119
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 92
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 92
- 125000004914 dipropylamino group Chemical group C(CC)N(CCC)* 0.000 claims 57
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 50
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims 48
- QZUPTXGVPYNUIT-UHFFFAOYSA-N isophthalamide Chemical compound NC(=O)C1=CC=CC(C(N)=O)=C1 QZUPTXGVPYNUIT-UHFFFAOYSA-N 0.000 claims 48
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 45
- IQZBKIANMUDLAR-UHFFFAOYSA-N C(CC)C1=CC(=C(C=C1C(=O)N)C(=O)N)CCC Chemical compound C(CC)C1=CC(=C(C=C1C(=O)N)C(=O)N)CCC IQZBKIANMUDLAR-UHFFFAOYSA-N 0.000 claims 43
- BTANRVKWQNVYAZ-UHFFFAOYSA-N 2-butanol Substances CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 claims 40
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 33
- 150000003839 salts Chemical class 0.000 claims 28
- LKJPYSCBVHEWIU-UHFFFAOYSA-N N-[4-cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)sulfonyl]-2-hydroxy-2-methylpropanamide Chemical compound C=1C=C(C#N)C(C(F)(F)F)=CC=1NC(=O)C(O)(C)CS(=O)(=O)C1=CC=C(F)C=C1 LKJPYSCBVHEWIU-UHFFFAOYSA-N 0.000 claims 26
- 235000010290 biphenyl Nutrition 0.000 claims 24
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 23
- YNTOKMNHRPSGFU-UHFFFAOYSA-N n-Propyl carbamate Chemical compound CCCOC(N)=O YNTOKMNHRPSGFU-UHFFFAOYSA-N 0.000 claims 23
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 23
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 22
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims 17
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 15
- 150000002576 ketones Chemical class 0.000 claims 14
- 239000004305 biphenyl Substances 0.000 claims 13
- 125000006480 iodobenzyl group Chemical group 0.000 claims 13
- 238000006467 substitution reaction Methods 0.000 claims 13
- 125000006185 3,4-dimethyl benzyl group Chemical group [H]C1=C(C([H])=C(C(=C1[H])C([H])([H])[H])C([H])([H])[H])C([H])([H])* 0.000 claims 12
- 125000004211 3,5-difluorophenyl group Chemical group [H]C1=C(F)C([H])=C(*)C([H])=C1F 0.000 claims 11
- 125000006180 3-methyl benzyl group Chemical group [H]C1=C([H])C(=C([H])C(=C1[H])C([H])([H])[H])C([H])([H])* 0.000 claims 11
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 11
- 125000006125 ethylsulfonyl group Chemical group 0.000 claims 11
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 11
- 125000006288 3,5-difluorobenzyl group Chemical group [H]C1=C(F)C([H])=C(C([H])=C1F)C([H])([H])* 0.000 claims 10
- 125000006279 3-bromobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(Br)=C1[H])C([H])([H])* 0.000 claims 10
- 125000006284 3-fluorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(F)=C1[H])C([H])([H])* 0.000 claims 10
- FVQBZTWIEXGMQV-UHFFFAOYSA-N 2-propylbenzene-1,3-dicarboxamide Chemical compound CCCC1=C(C(N)=O)C=CC=C1C(N)=O FVQBZTWIEXGMQV-UHFFFAOYSA-N 0.000 claims 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 9
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- 208000027061 mild cognitive impairment Diseases 0.000 claims 9
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims 8
- 208000005145 Cerebral amyloid angiopathy Diseases 0.000 claims 8
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims 8
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 8
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- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims 7
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- 125000006184 2,5-dimethyl benzyl group Chemical group [H]C1=C(C([H])=C(C(=C1[H])C([H])([H])[H])C([H])([H])*)C([H])([H])[H] 0.000 claims 6
- 125000006186 3,5-dimethyl benzyl group Chemical group [H]C1=C(C([H])=C(C([H])=C1C([H])([H])[H])C([H])([H])*)C([H])([H])[H] 0.000 claims 6
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- 125000006201 3-phenylpropyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 6
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- GKIRPKYJQBWNGO-OCEACIFDSA-N clomifene Chemical compound C1=CC(OCCN(CC)CC)=CC=C1C(\C=1C=CC=CC=1)=C(\Cl)C1=CC=CC=C1 GKIRPKYJQBWNGO-OCEACIFDSA-N 0.000 claims 6
- 230000003412 degenerative effect Effects 0.000 claims 6
- JNCMFHHNNWIPTH-LMSSTIIKSA-N n-[(2s,3r)-1-(3,5-difluorophenyl)-3-hydroxy-4-[(3-methoxyphenyl)methylamino]butan-2-yl]-1-propylindole-6-carboxamide Chemical compound C([C@H](NC(=O)C1=CC=C2C=CN(C2=C1)CCC)[C@H](O)CNCC=1C=C(OC)C=CC=1)C1=CC(F)=CC(F)=C1 JNCMFHHNNWIPTH-LMSSTIIKSA-N 0.000 claims 6
- 125000005301 thienylmethyl group Chemical group [H]C1=C([H])C([H])=C(S1)C([H])([H])* 0.000 claims 6
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- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 5
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims 5
- 125000002927 2-methoxybenzyl group Chemical group [H]C1=C([H])C([H])=C(C(OC([H])([H])[H])=C1[H])C([H])([H])* 0.000 claims 4
- 125000006179 2-methyl benzyl group Chemical group [H]C1=C([H])C(=C(C([H])=C1[H])C([H])([H])*)C([H])([H])[H] 0.000 claims 4
- 125000005806 3,4,5-trimethoxybenzyl group Chemical group [H]C1=C(OC([H])([H])[H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1C([H])([H])* 0.000 claims 4
- FPOKQPOBOUXHML-IZZNHLLZSA-N 3-(dipropylsulfamoyl)-n-[(2s,3r)-3-hydroxy-4-[(3-methoxyphenyl)methylamino]-1-phenylbutan-2-yl]propanamide Chemical compound C([C@H](NC(=O)CCS(=O)(=O)N(CCC)CCC)[C@H](O)CNCC=1C=C(OC)C=CC=1)C1=CC=CC=C1 FPOKQPOBOUXHML-IZZNHLLZSA-N 0.000 claims 4
- BIUDHHGROGJSHN-UHFFFAOYSA-N 4-fluoro-3-(trifluoromethyl)benzaldehyde Chemical group FC1=CC=C(C=O)C=C1C(F)(F)F BIUDHHGROGJSHN-UHFFFAOYSA-N 0.000 claims 4
- SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 claims 4
- 125000004217 4-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C([H])([H])* 0.000 claims 4
- 125000003352 4-tert-butyl benzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])*)C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 4
- 208000018282 ACys amyloidosis Diseases 0.000 claims 4
- 208000007487 Familial Cerebral Amyloid Angiopathy Diseases 0.000 claims 4
- 208000032849 Hereditary cerebral hemorrhage with amyloidosis Diseases 0.000 claims 4
- 239000002253 acid Substances 0.000 claims 4
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 4
- 210000004558 lewy body Anatomy 0.000 claims 4
- MSIWDEDJWPROJG-JHOUSYSJSA-N methyl 3-[[[(2r,3s)-4-(3,5-difluorophenyl)-3-[[3-(dipropylcarbamoyl)-5-methylbenzoyl]amino]-2-hydroxybutyl]amino]methyl]-1h-indole-6-carboxylate Chemical compound CCCN(CCC)C(=O)C1=CC(C)=CC(C(=O)N[C@@H](CC=2C=C(F)C=C(F)C=2)[C@H](O)CNCC=2C3=CC=C(C=C3NC=2)C(=O)OC)=C1 MSIWDEDJWPROJG-JHOUSYSJSA-N 0.000 claims 4
- JHMNNTDLYYZNNI-IOWSJCHKSA-N methyl 4-[[[(2r,3s)-4-(3,5-difluorophenyl)-3-[[3-(dipropylcarbamoyl)-5-methylbenzoyl]amino]-2-hydroxybutyl]amino]methyl]benzoate Chemical compound CCCN(CCC)C(=O)C1=CC(C)=CC(C(=O)N[C@@H](CC=2C=C(F)C=C(F)C=2)[C@H](O)CNCC=2C=CC(=CC=2)C(=O)OC)=C1 JHMNNTDLYYZNNI-IOWSJCHKSA-N 0.000 claims 4
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- BYKJARGIPRLCNK-LOSJGSFVSA-N n-[(2s,3r)-1-(3,5-difluorophenyl)-3-hydroxy-4-[(3-iodophenyl)methylamino]butan-2-yl]-5-oxo-5-piperidin-1-ylpentanamide Chemical compound C([C@@H](O)[C@H](CC=1C=C(F)C=C(F)C=1)NC(=O)CCCC(=O)N1CCCCC1)NCC1=CC=CC(I)=C1 BYKJARGIPRLCNK-LOSJGSFVSA-N 0.000 claims 4
- UYNVMTUALPULTH-XZWHSSHBSA-N n-[(2s,3r)-1-(3,5-difluorophenyl)-3-hydroxy-4-[(3-methoxyphenyl)methylamino]butan-2-yl]-3-phenylbenzamide Chemical compound COC1=CC=CC(CNC[C@@H](O)[C@H](CC=2C=C(F)C=C(F)C=2)NC(=O)C=2C=C(C=CC=2)C=2C=CC=CC=2)=C1 UYNVMTUALPULTH-XZWHSSHBSA-N 0.000 claims 4
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 claims 4
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- SCFRWIVEQMIEGJ-QUZSXMHDSA-N (1s,3r)-5-[[(2r,3s)-4-(3,5-difluorophenyl)-3-[[3-(dipropylcarbamoyl)-5-methylbenzoyl]amino]-2-hydroxybutyl]amino]cyclohexane-1,3-dicarboxylic acid Chemical compound CCCN(CCC)C(=O)C1=CC(C)=CC(C(=O)N[C@@H](CC=2C=C(F)C=C(F)C=2)[C@H](O)CNC2C[C@H](C[C@H](C2)C(O)=O)C(O)=O)=C1 SCFRWIVEQMIEGJ-QUZSXMHDSA-N 0.000 claims 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N 1-butanol Substances CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims 3
- FCQUHBYSDVGWPK-XZWHSSHBSA-N 1-n-[(2s,3r)-1-cyclohexyl-3-hydroxy-4-[(3-methoxyphenyl)methylamino]butan-2-yl]-3-n,3-n-dipropylbenzene-1,3,5-tricarboxamide Chemical compound CCCN(CCC)C(=O)C1=CC(C(N)=O)=CC(C(=O)N[C@@H](CC2CCCCC2)[C@H](O)CNCC=2C=C(OC)C=CC=2)=C1 FCQUHBYSDVGWPK-XZWHSSHBSA-N 0.000 claims 3
- 125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 claims 3
- UFDFOSSPKKCPOL-UHFFFAOYSA-N 2,4-dipropylbenzene-1,3,5-tricarboxamide Chemical compound CCCC1=C(C(N)=O)C=C(C(N)=O)C(CCC)=C1C(N)=O UFDFOSSPKKCPOL-UHFFFAOYSA-N 0.000 claims 3
- FDOJXWDDUDKIFU-UHFFFAOYSA-N 2-(dipropylcarbamoyl)benzoic acid Chemical compound CCCN(CCC)C(=O)C1=CC=CC=C1C(O)=O FDOJXWDDUDKIFU-UHFFFAOYSA-N 0.000 claims 3
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 claims 3
- 125000006282 2-chlorobenzyl group Chemical group [H]C1=C([H])C(Cl)=C(C([H])=C1[H])C([H])([H])* 0.000 claims 3
- 125000006509 3,4-difluorobenzyl group Chemical group [H]C1=C(F)C(F)=C([H])C(=C1[H])C([H])([H])* 0.000 claims 3
- MTLIEEHDEXXWGN-BJKOFHAPSA-N 3,5-difluoro-n-[(2s,3r)-3-hydroxy-4-[(3-methoxyphenyl)methylamino]-1-phenylbutan-2-yl]benzamide Chemical compound COC1=CC=CC(CNC[C@@H](O)[C@H](CC=2C=CC=CC=2)NC(=O)C=2C=C(F)C=C(F)C=2)=C1 MTLIEEHDEXXWGN-BJKOFHAPSA-N 0.000 claims 3
- IWNOPCMVDCWTKK-AJQTZOPKSA-N 3-(azepane-1-carbonyl)-n-[(2s,3r)-1-(3,5-difluorophenyl)-4-[(3-ethylphenyl)methylamino]-3-hydroxybutan-2-yl]-5-methylbenzamide Chemical compound CCC1=CC=CC(CNC[C@@H](O)[C@H](CC=2C=C(F)C=C(F)C=2)NC(=O)C=2C=C(C=C(C)C=2)C(=O)N2CCCCCC2)=C1 IWNOPCMVDCWTKK-AJQTZOPKSA-N 0.000 claims 3
- ZOCXTTPRZNKAEC-JGIBFQFJSA-N 3-[cyclohexyl(hydroxy)methyl]-n-[(2s,3r)-1-(3,5-difluorophenyl)-3-hydroxy-4-[(3-methoxyphenyl)methylamino]butan-2-yl]-5-methylbenzamide Chemical compound COC1=CC=CC(CNC[C@@H](O)[C@H](CC=2C=C(F)C=C(F)C=2)NC(=O)C=2C=C(C=C(C)C=2)C(O)C2CCCCC2)=C1 ZOCXTTPRZNKAEC-JGIBFQFJSA-N 0.000 claims 3
- VKASPRGMXGIRCO-IZZNHLLZSA-N 3-acetamido-n-[(2s,3r)-3-hydroxy-4-[(3-methoxyphenyl)methylamino]-1-phenylbutan-2-yl]benzamide Chemical compound COC1=CC=CC(CNC[C@@H](O)[C@H](CC=2C=CC=CC=2)NC(=O)C=2C=C(NC(C)=O)C=CC=2)=C1 VKASPRGMXGIRCO-IZZNHLLZSA-N 0.000 claims 3
- 125000000981 3-amino-3-oxopropyl group Chemical group [H]C([*])([H])C([H])([H])C(=O)N([H])[H] 0.000 claims 3
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- 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 claims 3
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- YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical class [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 claims 3
- DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 claims 3
- 150000007513 acids Chemical class 0.000 claims 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 3
- 125000000440 benzylamino group Chemical group [H]N(*)C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 3
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- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 3
- ACYGYJFTZSAZKR-UHFFFAOYSA-J dicalcium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Ca+2].[Ca+2].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O ACYGYJFTZSAZKR-UHFFFAOYSA-J 0.000 claims 3
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- XCFURYZGUYZVSE-AJQTZOPKSA-N ethyl 3-(dipropylcarbamoyl)-5-[[(2s,3r)-3-hydroxy-4-[(3-methoxyphenyl)methylamino]-1-phenylbutan-2-yl]carbamoyl]benzoate Chemical compound CCOC(=O)C1=CC(C(=O)N(CCC)CCC)=CC(C(=O)N[C@@H](CC=2C=CC=CC=2)[C@H](O)CNCC=2C=C(OC)C=CC=2)=C1 XCFURYZGUYZVSE-AJQTZOPKSA-N 0.000 claims 3
- 238000000338 in vitro Methods 0.000 claims 3
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- 230000035772 mutation Effects 0.000 claims 3
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- OSAZYHNTBSGFCS-JTHBVZDNSA-N n-[(2s,3r)-1-(3,5-difluorophenyl)-4-[(3-ethylphenyl)methylamino]-3-hydroxybutan-2-yl]-2-(ethylsulfonylamino)-1,3-oxazole-4-carboxamide Chemical compound CCC1=CC=CC(CNC[C@@H](O)[C@H](CC=2C=C(F)C=C(F)C=2)NC(=O)C=2N=C(NS(=O)(=O)CC)OC=2)=C1 OSAZYHNTBSGFCS-JTHBVZDNSA-N 0.000 claims 3
- DYSXWELOSAMCCY-IOWSJCHKSA-N n-[(2s,3r)-1-(3,5-difluorophenyl)-4-[(3-ethylphenyl)methylamino]-3-hydroxybutan-2-yl]-3-(4-hydroxypiperidine-1-carbonyl)-5-methylbenzamide Chemical compound CCC1=CC=CC(CNC[C@@H](O)[C@H](CC=2C=C(F)C=C(F)C=2)NC(=O)C=2C=C(C=C(C)C=2)C(=O)N2CCC(O)CC2)=C1 DYSXWELOSAMCCY-IOWSJCHKSA-N 0.000 claims 3
- MGHFZYNFTKAGQW-URLMMPGGSA-N n-[(2s,3r)-1-(3,5-difluorophenyl)-4-[(3-ethylphenyl)methylamino]-3-hydroxybutan-2-yl]-3-methyl-5-[(2-methylpropan-2-yl)oxy]benzamide Chemical compound CCC1=CC=CC(CNC[C@@H](O)[C@H](CC=2C=C(F)C=C(F)C=2)NC(=O)C=2C=C(OC(C)(C)C)C=C(C)C=2)=C1 MGHFZYNFTKAGQW-URLMMPGGSA-N 0.000 claims 3
- ZWNMRMJSGJSRGO-LMSSTIIKSA-N n-[(2s,3r)-1-(3,5-difluorophenyl)-4-[(3-ethylphenyl)methylamino]-3-hydroxybutan-2-yl]-4-hydroxy-3-(morpholine-4-carbonyl)benzamide Chemical compound CCC1=CC=CC(CNC[C@@H](O)[C@H](CC=2C=C(F)C=C(F)C=2)NC(=O)C=2C=C(C(O)=CC=2)C(=O)N2CCOCC2)=C1 ZWNMRMJSGJSRGO-LMSSTIIKSA-N 0.000 claims 3
- SMLVXBNXOPJWBZ-RRPNLBNLSA-N n-[(2s,3r)-3-hydroxy-4-[(3-methoxyphenyl)methylamino]-1-phenylbutan-2-yl]-1,3-dioxo-2-propylisoindole-5-carboxamide Chemical compound C([C@H](NC(=O)C1=CC=C2C(=O)N(C(C2=C1)=O)CCC)[C@H](O)CNCC=1C=C(OC)C=CC=1)C1=CC=CC=C1 SMLVXBNXOPJWBZ-RRPNLBNLSA-N 0.000 claims 3
- UXHCFADXHYMNDF-IZZNHLLZSA-N n-[(2s,3r)-3-hydroxy-4-[(3-methoxyphenyl)methylamino]-1-phenylbutan-2-yl]-2-methyl-3h-benzimidazole-5-carboxamide Chemical compound COC1=CC=CC(CNC[C@@H](O)[C@H](CC=2C=CC=CC=2)NC(=O)C=2C=C3N=C(C)NC3=CC=2)=C1 UXHCFADXHYMNDF-IZZNHLLZSA-N 0.000 claims 3
- STACDKIZZOHKEX-VQTJNVASSA-N n-[(2s,3r)-3-hydroxy-4-[(3-methoxyphenyl)methylamino]-1-phenylbutan-2-yl]acetamide Chemical compound COC1=CC=CC(CNC[C@@H](O)[C@H](CC=2C=CC=CC=2)NC(C)=O)=C1 STACDKIZZOHKEX-VQTJNVASSA-N 0.000 claims 3
- YUHZMEOAHNCYKZ-RRPNLBNLSA-N n-[(2s,3r)-4-(benzylamino)-1-(3,5-difluorophenyl)-3-hydroxybutan-2-yl]-3-(morpholine-4-carbonyl)benzamide Chemical compound C([C@@H](O)[C@H](CC=1C=C(F)C=C(F)C=1)NC(=O)C=1C=C(C=CC=1)C(=O)N1CCOCC1)NCC1=CC=CC=C1 YUHZMEOAHNCYKZ-RRPNLBNLSA-N 0.000 claims 3
- NYKMGHHEQHJAFX-WUFINQPMSA-N n-[(2s,3r)-4-[(3-cyclopropylphenyl)methylamino]-1-(3,5-difluorophenyl)-3-hydroxybutan-2-yl]-3-(dipropylsulfamoyl)propanamide Chemical compound C([C@H](NC(=O)CCS(=O)(=O)N(CCC)CCC)[C@H](O)CNCC=1C=C(C=CC=1)C1CC1)C1=CC(F)=CC(F)=C1 NYKMGHHEQHJAFX-WUFINQPMSA-N 0.000 claims 3
- 125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 claims 3
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 3
- BSCCSDNZEIHXOK-UHFFFAOYSA-N phenyl carbamate Chemical compound NC(=O)OC1=CC=CC=C1 BSCCSDNZEIHXOK-UHFFFAOYSA-N 0.000 claims 3
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 claims 3
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 3
- WGKIHPLAOHREFM-KHPTUGONSA-N (1s,2r,3r)-n-[(2s,3r)-1-(3,5-difluorophenyl)-3-hydroxy-4-[(3-methoxyphenyl)methylamino]butan-2-yl]-2-[2-(dipropylamino)-2-oxoethyl]-3-phenylcyclopropane-1-carboxamide Chemical compound C1([C@H]2[C@H]([C@@H]2CC(=O)N(CCC)CCC)C(=O)N[C@@H](CC=2C=C(F)C=C(F)C=2)[C@H](O)CNCC=2C=C(OC)C=CC=2)=CC=CC=C1 WGKIHPLAOHREFM-KHPTUGONSA-N 0.000 claims 2
- NEWXQDZIAABUJJ-CQTOTRCISA-N 1-heptan-4-yl-n-[(2s,3r)-3-hydroxy-4-[(3-methoxyphenyl)methylamino]-1-phenylbutan-2-yl]indole-6-carboxamide Chemical compound C([C@H](NC(=O)C1=CC=C2C=CN(C2=C1)C(CCC)CCC)[C@H](O)CNCC=1C=C(OC)C=CC=1)C1=CC=CC=C1 NEWXQDZIAABUJJ-CQTOTRCISA-N 0.000 claims 2
- XDLPXGGDOZPRDD-IZZNHLLZSA-N 1-n-[(2r,3s)-1-(benzylamino)-2-hydroxyhex-5-yn-3-yl]-5-methyl-3-n,3-n-dipropylbenzene-1,3-dicarboxamide Chemical compound CCCN(CCC)C(=O)C1=CC(C)=CC(C(=O)N[C@@H](CC#C)[C@H](O)CNCC=2C=CC=CC=2)=C1 XDLPXGGDOZPRDD-IZZNHLLZSA-N 0.000 claims 2
- ZKCURGPTJUZPRF-UKILVPOCSA-N 1-n-[(2s,3r)-1-(3,5-difluorophenyl)-3-hydroxy-4-[(3-iodophenyl)methylamino]butan-2-yl]-3-n-ethyl-4-hydroxybenzene-1,3-dicarboxamide Chemical compound C1=C(O)C(C(=O)NCC)=CC(C(=O)N[C@@H](CC=2C=C(F)C=C(F)C=2)[C@H](O)CNCC=2C=C(I)C=CC=2)=C1 ZKCURGPTJUZPRF-UKILVPOCSA-N 0.000 claims 2
- AGRNSQNIEMGHTN-IOWSJCHKSA-N 1-n-[(2s,3r)-1-(3-chlorophenyl)-3-hydroxy-4-[(3-methoxyphenyl)methylamino]butan-2-yl]-5-methyl-3-n,3-n-dipropylbenzene-1,3-dicarboxamide Chemical compound CCCN(CCC)C(=O)C1=CC(C)=CC(C(=O)N[C@@H](CC=2C=C(Cl)C=CC=2)[C@H](O)CNCC=2C=C(OC)C=CC=2)=C1 AGRNSQNIEMGHTN-IOWSJCHKSA-N 0.000 claims 2
- HRHHARZIDINHKP-AJQTZOPKSA-N 1-n-[(2s,3r)-3-hydroxy-1-(4-methoxyphenyl)-4-[(3-methoxyphenyl)methylamino]butan-2-yl]-5-methyl-3-n,3-n-dipropylbenzene-1,3-dicarboxamide Chemical compound CCCN(CCC)C(=O)C1=CC(C)=CC(C(=O)N[C@@H](CC=2C=CC(OC)=CC=2)[C@H](O)CNCC=2C=C(OC)C=CC=2)=C1 HRHHARZIDINHKP-AJQTZOPKSA-N 0.000 claims 2
- YESLVPQZUXMJHH-WUFINQPMSA-N 2-(dipropylamino)-n-[(2s,3r)-3-hydroxy-4-[(3-methoxyphenyl)methylamino]-1-phenylbutan-2-yl]pyridine-4-carboxamide Chemical compound C1=NC(N(CCC)CCC)=CC(C(=O)N[C@@H](CC=2C=CC=CC=2)[C@H](O)CNCC=2C=C(OC)C=CC=2)=C1 YESLVPQZUXMJHH-WUFINQPMSA-N 0.000 claims 2
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Classifications
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- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/13—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
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- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
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- C07C235/84—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups and doubly-bound oxygen atoms bound to the same carbon skeleton with the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
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- 2001-06-29 JP JP2002507763A patent/JP2004502665A/ja active Pending
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