KR920701178A - 3-아릴옥사졸리디논 유도체, 그의 제조방법 및 그의 치료 용도 - Google Patents
3-아릴옥사졸리디논 유도체, 그의 제조방법 및 그의 치료 용도Info
- Publication number
- KR920701178A KR920701178A KR1019910700620A KR910700620A KR920701178A KR 920701178 A KR920701178 A KR 920701178A KR 1019910700620 A KR1019910700620 A KR 1019910700620A KR 910700620 A KR910700620 A KR 910700620A KR 920701178 A KR920701178 A KR 920701178A
- Authority
- KR
- South Korea
- Prior art keywords
- oxygen
- compound
- derivatives
- alkyl
- formula
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
-
- 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
-
- 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
-
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D263/16—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
- C07D263/18—Oxygen atoms
- C07D263/20—Oxygen atoms attached in position 2
- C07D263/24—Oxygen atoms attached in position 2 with hydrocarbon radicals, substituted by oxygen atoms, attached to other ring carbon atoms
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (13)
- 부분입체 이성질체나 거울상 이성질체형 또는 시스-나 트랜스-형 또는 R1=CH3, X=산소, R2=R2'=H, n=1 또는 2 및 O=산소인 라세미체를 제외한 라세미형을 포함한 이들 모든형의 혼합물형의 다음 식(Ⅰ)의 유도체들.상기식에서, -R1는 수소 또는 C1-C4알킬; -X는 산소원자, 메틸렌 기 또는 -CH=CH-기; -n은 X가 산소원자 또는 메틸렌기 일때는 1또는 2, X가 -CH=CH-기 일때는 0 또는 1; -D는산소원자 또는 NOR기, 여기서, R=수소 또는 C1-C4알킬; -R3는 C1-C4알킬, C3-C7사이클로알킬, 페닐 또는 벤질기; -R2, R2' 각각은 독립적으로 수소원자 또는 C1-C4알킬, C3-C7사이클로알킬, 페닐 또는 벤질기; 및 -R2'와 R3는 또한 함께 -(CH2)3- 또는 -(CH2)4- 사슬을 형성할 수 있다.
- 제1항에 있어서, -R1=H 또는 CH3; -X=산소 또는 CH2; -n=1 또는 2; -R2=R2'=H 또는 CH3; -R3=C1-C4알킬; 및 -D는 산소, N-HO 또는 N-OCH3인 유도체들.
- 제1항에 있어서, -R1=CH3; -X=산소; -n=1 또는 2; -R2=R2'=H; -R3=CH3; 및 -D는 산소인 유도체들.
- 제1항에 있어서, -R1=CH3; -X=산소; -n=1 또는 2; -R2=R2'=H; -R3=CH3; 및 -D는 (E) N-OH인 유도체들.
- 제1항에 있어서, -R1=CH3; -X=메틸렌; -n=1 또는 2; -R2=R2'=H; -R3=CH3; 및 -D는 산소인 유도체들.
- 제1항에 있어서, -R1=CH3; -X=메틸렌; -n=1 또는 2; -R2=R2'=H; -R3=CH3; 및 -D는 (E) N-OH인 유도체들.
- 제1항에 있어서, -R1=CH3; -X는 -CH=CH-; -n=O 또는 1; -R2=R2'=H; -R3=CH3; 및 -D는 산소인 유도체들.
- 제1항에 있어서, -R1=CH3; -X는 -CH=CH-; -n=O 또는 1; -R2=R2'=H; -R3=CH3; 및 -D는(E) N-OH인 유도체들.
- 제1항에 있어서, R1=CH3; X=메틸렌; n=1; -R2=R2'=H; -R3=CH3; 및 -D는 산소인 유도체.
- 제3항 내지 제9항에 있어서, 비대칭 탄소원자가 (R) 구조를 갖는 유도체.
- 생리학적으로 허용될 수 있는 부형제와 제1항 내지 제10항 중의 어느 하나에 의한 화합물들 중에서 선택된 최소한 하나의 화합물을 포함하는 것을 특징으로 하는 제약 조성물.
- 의약의 제조를 위한, 제1항 내지 제10항에 의한 유도체들이 용도.
- a) 다음식의 화합물들을 가수분해시킴:(상기 식에서, R1, X, n, R2, R2' 및 R3는 식(Ⅰ)에서와 같은 의미를 갖고, R4와 R4' 각각은 독립적으로 C1-C4알킬이거나 R4와 R4'는 함께 -(CH2)2- 또는 -(CH2)3- 사슬을 형성한다) b) 다음 식의 화합물을 산화시킴(상기 식에서, 다른 매개변수들은 식(Ⅰ)에서와 같은 의미를 갖는다) c) C1-C4알킬 카보네이트를 다음식의 화합물과 축합반응시킴:(상기 식에서, n, X, R2, R2' 및 R3는 식(Ⅰ)에서와 같은 의미를 같은 의미를 갖는다)또는 d) 다음 식의 C1-C4알킬 할로게나이드 화합물과 알킬화시킴:(상기 식에서, n, X, R2, R2' 및 R3는 식(Ⅰ)에서와 같은 의미를 갖는다)을 특징으로 하는 제1항에 따른 식(Ⅰ)의 유도체들의 제조방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8913555A FR2653017B1 (fr) | 1989-10-17 | 1989-10-17 | Derives d'aryl-3 oxazolidinone-2, leur procede de preparation et leur application en therapeutique. |
FR8913555 | 1989-10-17 | ||
PCT/FR1990/000747 WO1991005776A1 (fr) | 1989-10-17 | 1990-10-17 | Aryl-3 oxazolidinones leur preparation et utilisation |
Publications (1)
Publication Number | Publication Date |
---|---|
KR920701178A true KR920701178A (ko) | 1992-08-11 |
Family
ID=9386480
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019910700619A KR0149508B1 (ko) | 1989-10-17 | 1990-10-17 | 3-아릴옥사졸리디논 유도체, 그의 제조 방법 및 그의 치료 용도 |
KR1019910700618A KR920701176A (ko) | 1989-10-17 | 1990-10-17 | 3-아릴옥사졸리디논 유도체, 그의 제조 방법 및 그의 치료 용도 |
KR1019910700620A KR920701178A (ko) | 1989-10-17 | 1990-10-17 | 3-아릴옥사졸리디논 유도체, 그의 제조방법 및 그의 치료 용도 |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019910700619A KR0149508B1 (ko) | 1989-10-17 | 1990-10-17 | 3-아릴옥사졸리디논 유도체, 그의 제조 방법 및 그의 치료 용도 |
KR1019910700618A KR920701176A (ko) | 1989-10-17 | 1990-10-17 | 3-아릴옥사졸리디논 유도체, 그의 제조 방법 및 그의 치료 용도 |
Country Status (16)
Country | Link |
---|---|
US (3) | US5036090A (ko) |
EP (3) | EP0428421A1 (ko) |
JP (3) | JPH04502333A (ko) |
KR (3) | KR0149508B1 (ko) |
AT (2) | ATE126220T1 (ko) |
AU (3) | AU637150B2 (ko) |
CA (3) | CA2027783C (ko) |
DE (2) | DE69021823T2 (ko) |
DK (1) | DK0424244T3 (ko) |
ES (1) | ES2078958T3 (ko) |
FR (1) | FR2653017B1 (ko) |
GR (1) | GR3017708T3 (ko) |
HK (1) | HK1005591A1 (ko) |
NZ (3) | NZ235728A (ko) |
WO (3) | WO1991005776A1 (ko) |
ZA (3) | ZA908283B (ko) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5235063A (en) * | 1989-10-17 | 1993-08-10 | Delalande S.A. | Process of preparing by condensation certain |
US5196543A (en) * | 1989-10-17 | 1993-03-23 | Delalande S.A. | 3-aryloxazolidinone derivatives, process for their preparation and their use in therapy |
FR2653017B1 (fr) * | 1989-10-17 | 1995-05-05 | Delalande Sa | Derives d'aryl-3 oxazolidinone-2, leur procede de preparation et leur application en therapeutique. |
FR2675504B1 (fr) * | 1991-04-16 | 1995-01-27 | Delalande Sa | Derives d'aryl-3 oxazolidinone, leur procede de preparation et leur application en therapeutique. |
TW286317B (ko) * | 1993-12-13 | 1996-09-21 | Hoffmann La Roche | |
FR2715155B1 (fr) * | 1994-01-19 | 1996-07-26 | Mayoly Spindler | Inhibiteurs de la monoamine oxydase B et leurs procédés de préparation. |
FR2732679B1 (fr) * | 1995-04-07 | 1997-04-30 | Synthelabo | Procede de preparation enzymatique d'un intermediaire de synthese de la befloxatone |
FR2734820B1 (fr) * | 1995-06-02 | 1997-07-11 | Synthelabo | Derives de 3-(1,2-benzisoxazol-3-yl)oxazolidin-2-one, leur preparation et leur application en therapeutique |
CN1075072C (zh) * | 1995-06-02 | 2001-11-21 | 圣诺菲—合成实验室公司 | 噁唑烷酮衍生物及其制法和用途 |
FR2734821B1 (fr) * | 1995-06-02 | 1997-07-11 | Synthelabo | Derives de 5-methoxymethyl-3-(1,2-benzisoxazol-3-yl) oxazolidin-2-one, leur preparation et leur application en therapeutique |
FR2737206B1 (fr) * | 1995-07-24 | 1997-08-22 | Synthelabo | Derives d'oxazoloquinoleinone, leur preparation et leur application en therapeutique |
FR2741072B1 (fr) * | 1995-11-09 | 1997-12-12 | Synthelabo | Derives d'oxazolidin-2-one, leur preparation et leur application en therapeutique |
FR2741071B1 (fr) * | 1995-11-09 | 1997-12-12 | Synthelabo | Derives de 3-(benzofuran-5-yl)oxazolidin-2-one, leur preparation et leur application en therapeutique |
US6642409B2 (en) | 2000-01-27 | 2003-11-04 | Central Glass Company, Limited | Process for producing 4,4,4-trifluoro-3-hydroxybutyric acid derivatives |
US6444813B2 (en) * | 2000-02-02 | 2002-09-03 | Pharmacia & Upjohn Company | Linezolid-crystal form II |
WO2002018354A1 (en) * | 2000-08-31 | 2002-03-07 | Abbott Laboratories | Oxazolidinones and their use as antibacterial agents |
EP2266590A3 (en) | 2002-02-22 | 2011-04-20 | Shire LLC | Active agent delivery sytems and methods for protecting and administering active agents |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
LU80081A1 (fr) * | 1977-08-26 | 1979-05-15 | Delalande Sa | Nouvelles hydroxymethyl-5 oxazolidinones-2,leur procede de preparation et leur application therapeutique |
FR2458547B2 (fr) * | 1978-06-09 | 1986-05-16 | Delalande Sa | Nouvelles n-aryle azolones, leur procede de preparation et leur application en therapeutique |
FR2506769A2 (fr) * | 1978-06-09 | 1982-12-03 | Delalande Sa | Para-((cyano-5 n pentyl-1) phenyl)-3 methoxymethyl-5 oxazolidinone-2, son procede de preparation et ses applications en therapeutique |
US4348393A (en) * | 1978-06-09 | 1982-09-07 | Delalande S.A. | N-Aryl oxazolidinones, oxazolidinethiones, pyrrolidinones, pyrrolidines and thiazolidinones |
CA1171865A (en) * | 1980-06-04 | 1984-07-31 | Alain Lacour | N-aryl azolone derivatives, the process for preparing the same and their application in therapeutics |
FR2608604B1 (fr) * | 1986-12-19 | 1989-04-28 | Delalande Sa | Derives 5-hydroxyethyles de l'oxazolidinone-2, leurs procedes de preparation et leurs applications en therapeutique |
FR2653017B1 (fr) * | 1989-10-17 | 1995-05-05 | Delalande Sa | Derives d'aryl-3 oxazolidinone-2, leur procede de preparation et leur application en therapeutique. |
-
1989
- 1989-10-17 FR FR8913555A patent/FR2653017B1/fr not_active Expired - Fee Related
-
1990
- 1990-10-15 US US07/597,426 patent/US5036090A/en not_active Expired - Fee Related
- 1990-10-15 US US07/597,583 patent/US5036091A/en not_active Expired - Lifetime
- 1990-10-16 DE DE69021823T patent/DE69021823T2/de not_active Expired - Fee Related
- 1990-10-16 CA CA002027783A patent/CA2027783C/en not_active Expired - Lifetime
- 1990-10-16 US US07/598,254 patent/US5171747A/en not_active Expired - Fee Related
- 1990-10-16 ES ES90402892T patent/ES2078958T3/es not_active Expired - Lifetime
- 1990-10-16 CA CA002027782A patent/CA2027782C/en not_active Expired - Fee Related
- 1990-10-16 AT AT90402892T patent/ATE126220T1/de not_active IP Right Cessation
- 1990-10-16 EP EP90402893A patent/EP0428421A1/fr not_active Withdrawn
- 1990-10-16 DE DE69021498T patent/DE69021498T2/de not_active Expired - Lifetime
- 1990-10-16 EP EP90402891A patent/EP0424243B1/fr not_active Expired - Lifetime
- 1990-10-16 DK DK90402892.5T patent/DK0424244T3/da active
- 1990-10-16 EP EP90402892A patent/EP0424244B1/fr not_active Expired - Lifetime
- 1990-10-16 CA CA002027715A patent/CA2027715A1/en not_active Abandoned
- 1990-10-16 AT AT90402891T patent/ATE126792T1/de active
- 1990-10-17 ZA ZA908283A patent/ZA908283B/xx unknown
- 1990-10-17 NZ NZ235728A patent/NZ235728A/en unknown
- 1990-10-17 ZA ZA908285A patent/ZA908285B/xx unknown
- 1990-10-17 NZ NZ235729A patent/NZ235729A/en unknown
- 1990-10-17 AU AU64713/90A patent/AU637150B2/en not_active Ceased
- 1990-10-17 JP JP2514787A patent/JPH04502333A/ja active Pending
- 1990-10-17 WO PCT/FR1990/000747 patent/WO1991005776A1/fr unknown
- 1990-10-17 KR KR1019910700619A patent/KR0149508B1/ko not_active IP Right Cessation
- 1990-10-17 JP JP2514789A patent/JPH04502335A/ja active Pending
- 1990-10-17 KR KR1019910700618A patent/KR920701176A/ko active IP Right Grant
- 1990-10-17 AU AU64714/90A patent/AU637413B2/en not_active Expired
- 1990-10-17 JP JP2514788A patent/JPH07103114B2/ja not_active Expired - Lifetime
- 1990-10-17 KR KR1019910700620A patent/KR920701178A/ko not_active Application Discontinuation
- 1990-10-17 ZA ZA908284A patent/ZA908284B/xx unknown
- 1990-10-17 AU AU64715/90A patent/AU635779B2/en not_active Ceased
- 1990-10-17 NZ NZ235727A patent/NZ235727A/en unknown
- 1990-10-17 WO PCT/FR1990/000746 patent/WO1991005775A1/fr active Application Filing
- 1990-10-17 WO PCT/FR1990/000745 patent/WO1991005774A1/fr unknown
-
1995
- 1995-10-11 GR GR950402817T patent/GR3017708T3/el unknown
-
1998
- 1998-06-02 HK HK98104744A patent/HK1005591A1/xx not_active IP Right Cessation
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WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |