KR830004300A - 벤조디아제핀 화합물의 제조방법 - Google Patents
벤조디아제핀 화합물의 제조방법 Download PDFInfo
- Publication number
- KR830004300A KR830004300A KR1019800003960A KR800003960A KR830004300A KR 830004300 A KR830004300 A KR 830004300A KR 1019800003960 A KR1019800003960 A KR 1019800003960A KR 800003960 A KR800003960 A KR 800003960A KR 830004300 A KR830004300 A KR 830004300A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- hydrogen
- cycloalkyl
- general formula
- halogen
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
- -1 benzodiazepine compound Chemical class 0.000 title claims 4
- 238000000034 method Methods 0.000 title claims 3
- 229940049706 benzodiazepine Drugs 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 claims 25
- 229910052739 hydrogen Inorganic materials 0.000 claims 21
- 239000001257 hydrogen Substances 0.000 claims 21
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 17
- 150000002431 hydrogen Chemical group 0.000 claims 16
- 150000001875 compounds Chemical class 0.000 claims 8
- 229910052736 halogen Inorganic materials 0.000 claims 8
- 150000002367 halogens Chemical class 0.000 claims 8
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 7
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
- 125000003342 alkenyl group Chemical group 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 125000004414 alkyl thio group Chemical group 0.000 claims 3
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 125000002861 (C1-C4) alkanoyl group Chemical group 0.000 claims 2
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 2
- 125000004442 acylamino group Chemical group 0.000 claims 2
- 150000001412 amines Chemical class 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 1
- 125000001589 carboacyl group Chemical group 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 125000003396 thiol group Chemical group [H]S* 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D231/38—Nitrogen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Anesthesiology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Otolaryngology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Description
Claims (7)
- (가) 일반식 R5H의 아민을 다음 일반식으로 표시되는 화합물과 반응시키거나여기서 Q는 아민 R5H의 수소원자를 분리할 수 있는 기를 나타내고, R6또는 R9이 수소이면 일반식 R6X 또는 R9X의 화합물과 반응시키고, X는 이탈기이고, n가 0이면 산화시킨다.(나) 다음 일반식의 화합물을 폐환시켜서 제조함을(R6와 R9가 수소이면, 일반식 R6X와 R9X와 반응시키고 X는 이탈기이고, n가 0이면 산화시킨다)특징으로 하는 하기 일반식(Ⅰ)으로 표시되는 화합물 또는 이의 산부가염의 제조방법.(상기 식에서 R1,R2,R3와 R10는 각각 수소, C1-4알킬, C2-4알켄일, C3-7싸이클로알킬, C3-7싸이클로알킬 C1-4알킬, 할로겐, C1-4할로알킬, C1-4알카노일, 니트로, 아미노, C2-4아실아미노, 시아노, 히드록실, C1-4알콕시, C1-4알킬티오, C1-4할로알콕시 또는 일반식 -SO2N(R8)2, -S02R8또는 -S03R8를 나타내고 여기서 R8은 C1-4알킬, C1-4할로알킬 또는 임의로 치환된 페닐이고; QR5는 다음 일반식의 기이다.여기서 R9는 할로겐, C1-4알킬, C3-7싸이클로알킬, C3-7싸이클로알킬, C1-4알킬, C1-4할로알킬, C2-4알켄일, C1-4알카노일, 벤질, 시아노- 또는 임의로 치환된 페닐이고 R10은 수소, C1-4알킬 또는 임의로 치환된 페닐이고, n는 0 또는 1이다; R6는 수소, C1-10알킬, C3-7싸이클로알킬, C3-7싸이클로알킬 C1-4알킬, C1-4할로알킬, 벤질, C1-6알카노일, C1-4카르브알콕시 또는 벤조일이고, R7은 R6중의 하나 또는 할로겐, 니트로, 시아노, 아미노 또는 C1-4아실아미노이다).
- R1,R2와 R3가 각각 수소, C1-4알킬, C2-4알켄일, 할로겐, C1-4할로알킬, 니트로, C1-4알콕시, C1-4할로알콕시, C1-4알킬티오, C1-4할로알킬설폰일 또는 페닐설폰일이고, R4는 수소이고, R6가 수소, C1-10알킬, C3-7싸이클로알킬, C3-7싸이클로알킬 C1-4알킬 또는 벤질이고, R7가 수소 또는 C1-10알킬이고, R9이 수소, C1-4알킬, C3-7싸이클로알킬, C3-7싸이클로알킬 C1-4알킬 또는 벤질이고, R10이 수소 또는 C1-4알킬인 화합물을 제조하기 위한 청구범위 1에 따른 방법.
- 다음 일반식의 화합물을 제조하기 위한 청구범위 1에 따른 방법.(상기식에서 R1,R2와 R3가 각각 수소, C1-4알킬, C2-4알켄일, 할로겐, C1-4할로알킬, 니트로, C1-4알콕시, C1-4알킬티오 또는 페닐설폰일이고, R6는 수소, C1-10알킬, C3-7싸이클로알킬, C3-7싸이클로알킬 C1-4알킬 또는 벤질이고, R7은 수소 또는 C1-10알킬이고, R9은 수소, C1-4알킬, C3-7싸이클로알킬, C3-7싸이클로알킬 C1-4알킬 또는 벤질을 나타낸다).
- R1,R2와 R3가 각각 수소, 할로겐 또는 C1-4할로알킬을 나타내고, R6가 C1-6알킬, C3-7싸이클로알킬 또는 C3-7싸이클로알킬 C1-4알킬이고, R7은 수소이고 R9는 수소, C1-4알킬, C3-7싸이클로알킬 C1-4알킬 또는 벤질인 화합물을 제조하기 위한 청구범위 3에 따른 방법.
- R2가 할로겐이고 R1과 R3가 수소이고 또한 R2와 R3가 할로겐이고, R1이 수소이고, R6가 메틸 또는 에틸이고 R7이 수소이고, R9이 메틸인 화합물을 제조하기 위한 청구범위 4에 따른 방법.
- 다음 일반식으로 표시되는 중격화합물(여기서 R1,R2,R3,R4,R6와 R7은 청구범위 1에 언급된 바와 같고, Q는 히드록실, 티올 또는 아미노이다).
- 다음 일반식으로 표시되는 중간화합물(여기서 R1에서 R7까지는 청구범위 1에 언급된 바와 같다)※ 참고사항 : 최초출S원 내용에 의하여 공개하는 것임.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1019840004388A KR850000472B1 (ko) | 1979-10-16 | 1984-07-24 | 벤조디아제핀 화합물의 제조방법 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB7935846 | 1979-10-16 | ||
| GB7935846 | 1979-10-16 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019840004388A Division KR850000472B1 (ko) | 1979-10-16 | 1984-07-24 | 벤조디아제핀 화합물의 제조방법 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR830004300A true KR830004300A (ko) | 1983-07-09 |
| KR850000471B1 KR850000471B1 (ko) | 1985-04-08 |
Family
ID=10508540
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019800003960A Expired KR850000471B1 (ko) | 1979-10-16 | 1980-10-15 | 벤조디아제핀 화합물의 제조 방법 |
| KR1019840004388A Expired KR850000472B1 (ko) | 1979-10-16 | 1984-07-24 | 벤조디아제핀 화합물의 제조방법 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019840004388A Expired KR850000472B1 (ko) | 1979-10-16 | 1984-07-24 | 벤조디아제핀 화합물의 제조방법 |
Country Status (33)
| Country | Link |
|---|---|
| US (3) | US4404137A (ko) |
| EP (1) | EP0027390B1 (ko) |
| JP (1) | JPS5663987A (ko) |
| KR (2) | KR850000471B1 (ko) |
| AR (2) | AR228041A1 (ko) |
| AT (1) | AT373889B (ko) |
| AU (1) | AU538500B2 (ko) |
| BE (1) | BE885729A (ko) |
| BG (2) | BG35042A3 (ko) |
| CA (1) | CA1159056A (ko) |
| CH (1) | CH646700A5 (ko) |
| CS (1) | CS244409B2 (ko) |
| DD (1) | DD153692A5 (ko) |
| DE (1) | DE3068706D1 (ko) |
| DK (1) | DK437480A (ko) |
| ES (1) | ES8106905A1 (ko) |
| FI (1) | FI67550C (ko) |
| FR (1) | FR2467851A1 (ko) |
| GB (1) | GB8327127D0 (ko) |
| GR (1) | GR70720B (ko) |
| HU (1) | HU182213B (ko) |
| IE (1) | IE50358B1 (ko) |
| IL (1) | IL61264A (ko) |
| IT (1) | IT1143047B (ko) |
| LU (1) | LU82853A1 (ko) |
| MX (1) | MX6233E (ko) |
| NZ (1) | NZ195248A (ko) |
| PH (2) | PH16288A (ko) |
| PL (2) | PL126824B1 (ko) |
| PT (1) | PT71913B (ko) |
| RO (2) | RO81351B (ko) |
| YU (1) | YU261580A (ko) |
| ZA (1) | ZA806342B (ko) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4404137A (en) * | 1979-10-16 | 1983-09-13 | Lilly Industries Limited | Pyrazolo [3,4-b][1,5]benzodiazepine compounds |
| US4431589A (en) * | 1980-12-11 | 1984-02-14 | Lilly House | Benzodiazepine compounds and their use as pharmaceuticals |
| US4596799A (en) * | 1985-01-29 | 1986-06-24 | Ciba-Geigy Corporation | 9H-pyrrolo[2,1-c]-1,2,4-triazolo[4,3-a][1,4]benzodiazepines |
| TW219896B (ko) * | 1988-07-07 | 1994-02-01 | Duphar Int Res | |
| GB8819059D0 (en) * | 1988-08-11 | 1988-09-14 | Lilly Industries Ltd | Benzodiazepine compounds & their use as pharmaceuticals |
| US5631250A (en) * | 1995-03-24 | 1997-05-20 | Eli Lilly And Company | Process and solvate of 2-methyl-thieno-benzodiazepine |
| US5637584A (en) * | 1995-03-24 | 1997-06-10 | Eli Lilly And Company | Solvate of olanzapine |
| US20050085463A1 (en) * | 2003-01-23 | 2005-04-21 | Weiner David M. | Use of N-desmethylclozapine to treat human neuropsychiatric disease |
| US20050250767A1 (en) * | 2003-01-23 | 2005-11-10 | Weiner David M | Use of N-desmethylclozapine to treat human neuropsychiatric disease |
| CN1741803A (zh) * | 2003-01-23 | 2006-03-01 | 阿卡蒂亚药品公司 | N-脱甲基氯氮平在治疗人神经精神疾病中的用途 |
| CA2550735A1 (en) * | 2003-12-22 | 2005-07-14 | Acadia Pharmaceuticals Inc. | Amino substituted diaryl[a,d]cycloheptene analogs as muscarinic agonists and methods of treatment of neuropsychiatric disorders |
| JP2007536216A (ja) * | 2004-04-01 | 2007-12-13 | アカディア ファーマシューティカルズ,インコーポレーテッド | 固体n−デスメチルクロザピンおよびその結晶形を合成および単離する方法 |
| WO2007053618A1 (en) * | 2005-10-31 | 2007-05-10 | Acadia Pharmaceuticals Inc. | Prodrugs of muscarinic agonists and methods of treatment of neuropsychiatric disorders |
| JP5438482B2 (ja) * | 2009-12-03 | 2014-03-12 | Juki株式会社 | ミシン、ミシンの縫製データ編集装置及びミシンの縫製データ編集プログラム |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3450694A (en) * | 1966-02-23 | 1969-06-17 | Abbott Lab | Substituted benzoxazepines and benzothiazepines |
| US3758479A (en) * | 1967-03-22 | 1973-09-11 | Sandoz Ag | Nitro and sulphamoyl substituted dibenzodiazepines |
| DE1795183B1 (de) * | 1968-08-20 | 1972-07-20 | Thomae Gmbh Dr K | 5,11-Dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-on-derivate und Arzneimittel |
| CA918659A (en) * | 1969-07-31 | 1973-01-09 | Yoshitomi Pharmaceutical Industries | 11-(4-substituted-1-piperazinyl)-dibenzo (b,f) (1,4) thiazepines |
| US4115568A (en) * | 1974-11-26 | 1978-09-19 | Lilly Industries Limited | Thieno[3,2-b]-[1,5]benzodiazepines |
| US4172831A (en) * | 1974-11-26 | 1979-10-30 | Lilly Industries Limited | Thieno-benzodiazepines |
| US3953430A (en) * | 1975-02-24 | 1976-04-27 | American Cyanamid Company | Substituted benzodiazepin-10-ones and method of use |
| US3951981A (en) * | 1975-02-24 | 1976-04-20 | American Cyanamid Company | Substituted benzodiazepines and method of use |
| DE2707270A1 (de) * | 1977-02-19 | 1978-08-24 | Hoechst Ag | Pyrazolo-diazepine und verfahren zu ihrer herstellung |
| DE2707269A1 (de) * | 1977-02-19 | 1978-08-24 | Hoechst Ag | Heterocyclische stickstoffverbindungen und verfahren zu ihrer herstellung |
| US4097597A (en) * | 1977-02-23 | 1978-06-27 | Abbott Laboratories | Dibenzo b,e! 1,4!diazepines |
| IT7851496A0 (it) * | 1977-10-31 | 1978-10-13 | Sandoz Ag | Menti pirazinobenzossazepine loro preparazione e loro impiego quali medica |
| CH643263A5 (de) * | 1979-05-11 | 1984-05-30 | Sandoz Ag | Benzodiazepine, ihre herstellung und verwendung. |
| EP0064775A1 (de) * | 1979-08-03 | 1982-11-17 | Byk Gulden Lomberg Chemische Fabrik GmbH | Substituierte Tetraazatricyclen, Verfahren zu ihrer Herstellung und ihre Verwendung |
| US4404137A (en) * | 1979-10-16 | 1983-09-13 | Lilly Industries Limited | Pyrazolo [3,4-b][1,5]benzodiazepine compounds |
-
1980
- 1980-10-02 US US06/193,200 patent/US4404137A/en not_active Expired - Lifetime
- 1980-10-11 GR GR63138A patent/GR70720B/el unknown
- 1980-10-13 RO RO102349A patent/RO81351B/ro unknown
- 1980-10-13 CS CS806938A patent/CS244409B2/cs unknown
- 1980-10-13 RO RO108967A patent/RO85822B/ro unknown
- 1980-10-13 YU YU02615/80A patent/YU261580A/xx unknown
- 1980-10-13 PH PH24717A patent/PH16288A/en unknown
- 1980-10-13 NZ NZ195248A patent/NZ195248A/xx unknown
- 1980-10-13 FR FR8021823A patent/FR2467851A1/fr active Granted
- 1980-10-13 MX MX809093U patent/MX6233E/es unknown
- 1980-10-13 IL IL61264A patent/IL61264A/xx unknown
- 1980-10-14 IT IT49899/80A patent/IT1143047B/it active
- 1980-10-14 CA CA000362328A patent/CA1159056A/en not_active Expired
- 1980-10-14 PT PT71913A patent/PT71913B/pt unknown
- 1980-10-14 CH CH763980A patent/CH646700A5/fr not_active IP Right Cessation
- 1980-10-14 AT AT0510180A patent/AT373889B/de not_active IP Right Cessation
- 1980-10-14 AU AU63252/80A patent/AU538500B2/en not_active Ceased
- 1980-10-15 ZA ZA00806342A patent/ZA806342B/xx unknown
- 1980-10-15 PL PL1980227306A patent/PL126824B1/pl unknown
- 1980-10-15 ES ES495948A patent/ES8106905A1/es not_active Expired
- 1980-10-15 IE IE2135/80A patent/IE50358B1/en unknown
- 1980-10-15 FI FI803253A patent/FI67550C/fi not_active IP Right Cessation
- 1980-10-15 KR KR1019800003960A patent/KR850000471B1/ko not_active Expired
- 1980-10-15 HU HU802502A patent/HU182213B/hu not_active IP Right Cessation
- 1980-10-15 JP JP14423180A patent/JPS5663987A/ja active Pending
- 1980-10-15 LU LU82853A patent/LU82853A1/fr unknown
- 1980-10-15 BG BG057344A patent/BG35042A3/xx unknown
- 1980-10-15 DD DD80224618A patent/DD153692A5/de unknown
- 1980-10-15 BG BG049366A patent/BG34907A3/xx unknown
- 1980-10-15 EP EP80303649A patent/EP0027390B1/en not_active Expired
- 1980-10-15 DK DK437480A patent/DK437480A/da not_active Application Discontinuation
- 1980-10-15 PL PL1980231270A patent/PL135044B1/pl unknown
- 1980-10-15 DE DE8080303649T patent/DE3068706D1/de not_active Expired
- 1980-10-15 BE BE6/47291A patent/BE885729A/fr not_active IP Right Cessation
- 1980-10-16 AR AR282893A patent/AR228041A1/es active
-
1982
- 1982-07-21 AR AR290034A patent/AR228101A1/es active
- 1982-07-28 PH PH27643A patent/PH17759A/en unknown
- 1982-09-29 US US06/426,580 patent/US4486591A/en not_active Expired - Fee Related
-
1983
- 1983-10-11 GB GB838327127A patent/GB8327127D0/en active Pending
-
1984
- 1984-07-24 KR KR1019840004388A patent/KR850000472B1/ko not_active Expired
- 1984-08-06 US US06/638,181 patent/US4542131A/en not_active Expired - Fee Related
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR830004300A (ko) | 벤조디아제핀 화합물의 제조방법 | |
| KR830007593A (ko) | 개선된 n-아릴벤즈아미드 유도체 | |
| KR840005083A (ko) | 항고혈압제로서 유용한 아미노산유도체의 제조방법 | |
| KR840006237A (ko) | 설포닐 우레아의 제조방법 | |
| KR950005827A (ko) | 신규 2- 아미노티아졸카르복사미드 유도체, 그의 제조방법 및 식물병원균 퇴치를 위한 그의 용도 | |
| KR840008155A (ko) | 트리아조로[4,3,-c] 피리미딘과 트리아조로[1,5-c]피리미딘의 제조방법 | |
| KR870000330A (ko) | 치환된 4,5-디하이드로-1,3,4-티아디아졸의 제조방법 | |
| KR840008323A (ko) | 5-아실-2-(1h)-피리디논의 제조방법 | |
| KR830007655A (ko) | 벤조디아제핀 화합물의 제조 방법 | |
| KR900003179A (ko) | 벤조디아제핀 화합물 및 약제로서의 이의 용도 | |
| KR860007232A (ko) | 벤조일 우레아의 제조방법 | |
| KR860008983A (ko) | 4- 벤조일-1- 알킬(알켄일) 피라졸의 제조방법 | |
| KR890008151A (ko) | 키놀린 카르복산의 유도체 | |
| KR850004745A (ko) | 1,2,4-옥사(티아)디아졸린-3-온 유도체의 제조방법 | |
| KR920012096A (ko) | 아스타크산틴 중간체 | |
| KR830009076A (ko) | 3,5-디-3급-부틸-4-하이드록시페닐-치환 복소환 화합물의 제조방법 | |
| KR840007656A (ko) | 살충제 조성물 | |
| KR870002093A (ko) | 설포닐이소(티오) 우레아의 제조방법 | |
| KR830008493A (ko) | 치환된 피리딘 1- 산화물 제초제 | |
| KR910000712A (ko) | 이미다졸 유도체의 제조방법 | |
| KR860007876A (ko) | 제초제 조성물 | |
| KR880005140A (ko) | 3-하이드록시-3-세펨 화합물의 제조방법 | |
| KR870005581A (ko) | 제초 조성물 | |
| KR830007573A (ko) | 피라졸 유도체의 제법 | |
| KR830003451A (ko) | 식물 생장 조절제로 유용한 2-옥소-3-벤조티아졸린 아세트산으로부터 유래된 이미드아미드 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 19801015 |
|
| PG1501 | Laying open of application | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 19840224 Patent event code: PE09021S01D |
|
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 19841114 Patent event code: PE09021S01D |
|
| PG1605 | Publication of application before grant of patent |
Comment text: Decision on Publication of Application Patent event code: PG16051S01I Patent event date: 19850305 |
|
| E701 | Decision to grant or registration of patent right | ||
| PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 19850626 |