KR850002097A - 2-메르캅토피리미도헥사하이드로퀴놀린 유도체의 제조방법 - Google Patents
2-메르캅토피리미도헥사하이드로퀴놀린 유도체의 제조방법 Download PDFInfo
- Publication number
- KR850002097A KR850002097A KR1019840005911A KR840005911A KR850002097A KR 850002097 A KR850002097 A KR 850002097A KR 1019840005911 A KR1019840005911 A KR 1019840005911A KR 840005911 A KR840005911 A KR 840005911A KR 850002097 A KR850002097 A KR 850002097A
- Authority
- KR
- South Korea
- Prior art keywords
- trans
- formula
- compound
- propyl
- alkyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 15
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims 16
- 150000001875 compounds Chemical class 0.000 claims 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 4
- MIYGGZBSUPJUSX-TZMCWYRMSA-N (4ar,8ar)-7-(dimethylaminomethylidene)-1-propyl-3,4,4a,5,8,8a-hexahydro-2h-quinolin-6-one Chemical compound C1C(=O)C(=CN(C)C)C[C@H]2N(CCC)CCC[C@@H]21 MIYGGZBSUPJUSX-TZMCWYRMSA-N 0.000 claims 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 2
- 230000007062 hydrolysis Effects 0.000 claims 2
- 238000006460 hydrolysis reaction Methods 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 239000007858 starting material Substances 0.000 claims 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims 2
- FWHLCAXBTREMQT-ZYHUDNBSSA-N (4ar,8ar)-1-propyl-2,3,4,4a,5,7,8,8a-octahydroquinolin-6-one Chemical compound C1C(=O)CC[C@H]2N(CCC)CCC[C@@H]21 FWHLCAXBTREMQT-ZYHUDNBSSA-N 0.000 claims 1
- YIHPFCVTYSQQNG-FZMZJTMJSA-N (5as,9as)-2-methylsulfanyl-6-propyl-5a,7,8,9,9a,10-hexahydro-5h-pyrido[2,3-g]quinazoline Chemical compound CSC1=NC=C2C[C@@H]3N(CCC)CCC[C@H]3CC2=N1 YIHPFCVTYSQQNG-FZMZJTMJSA-N 0.000 claims 1
- JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical compound C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 claims 1
- AVIZXGITNZAUHR-GDBMZVCRSA-N C(CC)N1CCC[C@@H]2CC(=CC[C@@H]12)N1CCCC1 Chemical compound C(CC)N1CCC[C@@H]2CC(=CC[C@@H]12)N1CCCC1 AVIZXGITNZAUHR-GDBMZVCRSA-N 0.000 claims 1
- 241001024304 Mino Species 0.000 claims 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 claims 1
- 230000003301 hydrolyzing effect Effects 0.000 claims 1
- RMAHPRNLQIRHIJ-UHFFFAOYSA-N methyl carbamimidate Chemical compound COC(N)=N RMAHPRNLQIRHIJ-UHFFFAOYSA-N 0.000 claims 1
- SDDKIZNHOCEXTF-UHFFFAOYSA-N methyl carbamimidothioate Chemical compound CSC(N)=N SDDKIZNHOCEXTF-UHFFFAOYSA-N 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 150000003672 ureas Chemical class 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/38—Nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Cosmetics (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (13)
- a) 일반식(Ⅲ)의 화합물을 일반식(Ⅶ)의 우레아 유도체로 폐환시켜 R1이 SH, S-C1-C3알킬 또는 O-C1-C3알킬이고 R2가 H인 일반식(Ⅰ)의 화합물을 수득하거나, b) 일반식(Ⅷ)의 화합물을 산으로 가수분해시켜 R1이 OH이고, R2가 H인 일반식(Ⅰ)의 화합물을 수득하거나, c) 일반식(Ⅸ)의 화합물을 일반식(Ⅹ)의 화합물로 폐환시켜 R1및 R2가 NH2인 일반식(Ⅰ)의 화합물을 수득하거나, d) 일반식(Ⅴ)의 화합물을 1,3,5-트리아진과 반응시켜 R1및 R2가 H인 일반식(Ⅰ)의 화합물을 수득하거나, e) 일반식(XI)의 화합물을 산으로 가수분해시켜 R이 H인 일반식(Ⅰ)의 화합물을 수득하거나, f) 임의로는, 일반식(Ⅰ)의 화합물을 염화함을 특징으로 하여 일반식(Ⅰ)의 화합물 또는 그의 약제학적으로 허용되는 염을 제조하는 방법.상기 식에서, R은 H, CN, C1-C3알킬 또는 알릴이고, R1은 H, OH, SH, NH2, O-C1-C3알킬 또는 S-C1-C3알킬이고 R2는 H 또는 NH2이며, 단 R2가 NH2일 경우에는 R1은 NH2이어야만 하고, R1a는 S-C1-C3알킬이고, X는 O,S, S-C1-C3알킬, 또는 O-C1-C3알킬이고, n은 1 또는 2이고, 점선은 2중결합을 표시한다.
- 제1항에 있어서, 형성된 생성물이 트란스-(-)-엔안티오머인 방법.
- 제1항 또는 2항에 있어서, R이 C1-C3알킬인 방법.
- 제1,2 또는 3항에 있어서, R2가 H인 방법.
- 제1항에 있어서, 공정 (a)에서, 트란스-(±)-1-n-프로필-6-옥소-7-디메틸아미노메틸렌데카하이드로퀴놀린을 티오우레아로 폐환시킴을 특징으로 하여 트란스-(±)-2-메르캅토-6-n-프로필-5,5a,6,7,8,9a,10-옥타하이드로피리미도[4,5-g]퀴놀린을 제조하는 방법.
- 제1항에 있어서, 공정 (a)에서, 트란스-(±)-1-n-프로필-6-옥소-7-디메틸아미노메틸렌데카하이드로퀴놀린을 S-메틸티오이소우레아로 폐환시킴을 특징으로 하여 트란스-(±)-2-6-n-프로필-5,5a,6,7,8,9a,10-옥타하이드로피리미도[4,5-g]퀴놀린을 제조하는 방법.
- 제1항에 있어서, 공정 (a)에서, 트란스-(±)-1-n-프로필-6-옥소-7-디메틸아미노메틸렌데카하이드로퀴놀린을 O-메틸이소우레아로 폐환시킴을 특징으로 하여 트란스-(±)-2-메톡시-6-n-프로필-5,5a,6,7,8,9a,10-옥타하이드로피리미도[4,5-g]퀴놀린을 제조하는 방법.
- 제1항에 있어서, 공정 (b)에서, 트란스-(±)-2-메틸티오-6-n-프로필-5,5a,6,7,8,9,9a,10-옥타하이드로피리미도[4,5-g]퀴놀린을 염산으로 가수분해시킴을 특징으로 하여 트란스-(±)-2-하이드록시-6-n-프로필-5,5a,6,7,8,9,9a,10-옥타하이드로피리미도[4,5-g]퀴놀린을 제조하는 방법.
- 제1항에 있어서, 공정 (c)에서, 트란스-(±)-1-n-프로필-6-옥소데카하이드로퀴놀린을 시아노구아니딘으로 폐환시킴을 특징으로 하여 트란스-(±)-2,4-디아미노-6-n-프로필-5,5a,6,7,8,9,9a,10-옥타하이드로피리미도[4,5-g]퀴놀린을 제조하는 방법.
- 제1항에 있어서, 공정 (d)에서, 트란스-(±)-1-n-프로필-6-피롤리디노-1,2,3,4,4a,5,8,8a-옥타하이드로퀴놀린을 1,3,5-트리아진과 반응시킴을 특징으로 하여 트란스-(±)-6-n-프로필-5,5a,6,7,8,9,9a,10-옥타하이드로피리미도[4,5-g]퀴놀린을 제조하는 방법.
- 제1항에 있어서, 공정 (e)에서, 트란스-(±)-6-시아노-2,4-디아미노-5,5a,6,7,8,9,9a,10-옥타하이드로피리미도[4,5-g]퀴놀린을 염산으로 가수분해시킴을 특징으로 하여 트란스-(±)-2,4-디아미노-5,5a,6,7,8,9,9a,10-옥타하이드로피리미도[4,5-g]퀴놀린을 제조하는 방법.
- 제1항에 있어서, 다음 일반식(Ⅴ)의 트란스-(±)-화합물을 출발물질로 사용하는 방법.상기 식에서 R은 C1-C3알킬 또는 알릴이다.
- 제1항에 있어서, 일반식(Ⅴ) 화학물 대신 다음 일반식(Ⅵ)의 트란스-(-)-화합물을 출발물질로 사용하는 방법.상기 식에서 R은 C1-C3알킬 또는 알릴이다.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/535,518 US4507478A (en) | 1983-09-26 | 1983-09-26 | 2-Mercaptopyrimidohexahydroquinolines and related compounds |
US535518 | 1983-09-26 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR850002097A true KR850002097A (ko) | 1985-05-06 |
KR870001160B1 KR870001160B1 (ko) | 1987-06-13 |
Family
ID=24134587
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019840005911A KR870001160B1 (ko) | 1983-09-26 | 1984-09-26 | 2-메르캅토 피리미도헥사하이드로퀴놀린 유도체의 제조방법 |
Country Status (12)
Country | Link |
---|---|
US (1) | US4507478A (ko) |
EP (1) | EP0138417B1 (ko) |
JP (2) | JPS60100580A (ko) |
KR (1) | KR870001160B1 (ko) |
CA (1) | CA1233177A (ko) |
DE (1) | DE3481615D1 (ko) |
DK (1) | DK451284A (ko) |
GB (1) | GB2146993B (ko) |
GR (1) | GR80411B (ko) |
HU (1) | HU193721B (ko) |
IE (1) | IE58095B1 (ko) |
IL (1) | IL73002A (ko) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4599339A (en) * | 1983-09-26 | 1986-07-08 | Eli Lilly And Company | Use of pyrimido[4,5-g]quinolines in treating parkinsonism |
RO89126A (ro) * | 1983-09-26 | 1986-04-30 | Eli Lilly And Co,Us | Procedeu de preparare a unor derivati de chinolina |
US4764609A (en) * | 1986-03-31 | 1988-08-16 | Eli Lilly And Company | Synthesis of 2-aminopyrimido[4,5-g]quinolines |
US5134143A (en) * | 1986-06-16 | 1992-07-28 | Eli Lilly And Company | BCD tricyclic ergoline part-structure analogues |
US4826986A (en) * | 1986-06-16 | 1989-05-02 | Eli Lilly And Company | 6-Oxo-trans-octa- and decahydroquinolines |
US4762843A (en) * | 1986-09-15 | 1988-08-09 | Warner-Lambert Company | Hetero [f] fused carbocyclic pyridines as dopaminergic agents |
US5416090A (en) * | 1991-01-31 | 1995-05-16 | Eli Lilly And Company | Method of treating inflammation |
DE4228455A1 (de) * | 1992-08-26 | 1994-09-15 | Beiersdorf Ag | Kosmetische und dermatologische Lichtschutzformulierungen mit einem Gehalt an Thiolen und/oder Thiolderivaten |
DE4242328C2 (de) * | 1992-12-15 | 1995-06-08 | Alfred Dipl Ing Dr Freissmuth | Mittel zur Entschwefelung, Entphosphorung, Entsilicierung und Entstickung von Roheisen- und Gußeisenschmelzen |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2794020A (en) * | 1953-08-03 | 1957-05-28 | Monsanto Chemicals | 6-amino substituted 1, 2, 3, 4-tetrahydroquinolines |
BE582178A (ko) * | 1958-09-02 | |||
US4198415A (en) * | 1979-01-22 | 1980-04-15 | Eli Lilly And Company | Prolactin inhibiting octahydro pyrazolo[3,4-g]quinolines |
JPS59177383A (ja) * | 1983-03-25 | 1984-10-08 | Mitsui Eng & Shipbuild Co Ltd | ステンレス鋼の応力腐食割れ防止構造 |
JPS63289902A (ja) * | 1987-05-22 | 1988-11-28 | Omron Tateisi Electronics Co | 可変抵抗器 |
-
1983
- 1983-09-26 US US06/535,518 patent/US4507478A/en not_active Expired - Fee Related
-
1984
- 1984-09-19 GR GR80411A patent/GR80411B/el unknown
- 1984-09-19 IL IL73002A patent/IL73002A/xx unknown
- 1984-09-19 CA CA000463536A patent/CA1233177A/en not_active Expired
- 1984-09-20 DE DE8484306434T patent/DE3481615D1/de not_active Expired - Lifetime
- 1984-09-20 EP EP84306434A patent/EP0138417B1/en not_active Expired
- 1984-09-20 GB GB08423850A patent/GB2146993B/en not_active Expired
- 1984-09-21 DK DK451284A patent/DK451284A/da not_active Application Discontinuation
- 1984-09-25 HU HU843615A patent/HU193721B/hu not_active IP Right Cessation
- 1984-09-25 IE IE244084A patent/IE58095B1/en not_active IP Right Cessation
- 1984-09-26 KR KR1019840005911A patent/KR870001160B1/ko not_active IP Right Cessation
- 1984-09-26 JP JP59202892A patent/JPS60100580A/ja active Granted
-
1992
- 1992-09-16 JP JP4246418A patent/JPH068291B2/ja not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH0528718B2 (ko) | 1993-04-27 |
HUT35263A (en) | 1985-06-28 |
KR870001160B1 (ko) | 1987-06-13 |
EP0138417A3 (en) | 1986-02-19 |
EP0138417A2 (en) | 1985-04-24 |
IL73002A0 (en) | 1984-12-31 |
CA1233177A (en) | 1988-02-23 |
GB8423850D0 (en) | 1984-10-24 |
JPS60100580A (ja) | 1985-06-04 |
IE58095B1 (en) | 1993-06-30 |
IE842440L (en) | 1985-03-26 |
GB2146993B (en) | 1987-07-08 |
IL73002A (en) | 1987-09-16 |
JPH05194488A (ja) | 1993-08-03 |
DK451284D0 (da) | 1984-09-21 |
JPH068291B2 (ja) | 1994-02-02 |
GR80411B (en) | 1985-01-16 |
EP0138417B1 (en) | 1990-03-14 |
DK451284A (da) | 1985-03-27 |
HU193721B (en) | 1987-11-30 |
GB2146993A (en) | 1985-05-01 |
DE3481615D1 (de) | 1990-04-19 |
US4507478A (en) | 1985-03-26 |
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