KR850003402A - 2-아미노-5-하이드록시-4-메틸 피리미딘 유도체의 제조방법 - Google Patents
2-아미노-5-하이드록시-4-메틸 피리미딘 유도체의 제조방법 Download PDFInfo
- Publication number
- KR850003402A KR850003402A KR1019840006093A KR840006093A KR850003402A KR 850003402 A KR850003402 A KR 850003402A KR 1019840006093 A KR1019840006093 A KR 1019840006093A KR 840006093 A KR840006093 A KR 840006093A KR 850003402 A KR850003402 A KR 850003402A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- general formula
- compound
- phenyl
- formula
- Prior art date
Links
- VCIHPVOAXJAJLZ-UHFFFAOYSA-N 2-amino-4-methylpyrimidin-5-ol Chemical class CC1=NC(N)=NC=C1O VCIHPVOAXJAJLZ-UHFFFAOYSA-N 0.000 title 1
- 125000006732 (C1-C15) alkyl group Chemical group 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 125000003884 phenylalkyl group Chemical group 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 125000005936 piperidyl group Chemical group 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims 1
- BXULNSJILNIAEU-UHFFFAOYSA-N 1-(2-amino-1,3-oxazol-5-yl)ethanone Chemical compound CC(=O)C1=CN=C(N)O1 BXULNSJILNIAEU-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
-
- 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
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
-
- 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
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole 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
- C07D263/48—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (1)
- 일반식(II)의 5-아세틸-2-아미노옥사졸을 물 존재하에 90℃ 내지 125℃ 범위의 온도에서 일반식 RR′NH의 아민과 반응시키고, 생성된 혼합물로 부터 목적하는 일반식(I)의 화합물을 분리시키고, 필요한 경우, 생성된 화합물을 적절한 산과 반응시켜 약제학적으로 허용되는 산부가염으로 전환시킴을 특징으로 하여 거의 순수한 형태의 다음 일반식(I)의 화합물 또는 그의 산부가염을 제조하는 방법.상기식에서, R은 수소 또는 (C1-C15)알킬이고, R′는 수소, (C1-C15)알킬, (C5-C8)시클로알킬, (C2-C15)알케닐, 페닐, 푸릴, 티에닐, (C7-C20)페닐알킬, 또는 할로, (C1-C3)알킬, (C1-C3)알콕시 또는 트리플루오로메틸에 의해 치환된 페닐 알킬이거나; R 및 R′는 이들이 부착된 질소원자와 함께 피페리딜그룹, (C1-C15)알킬 또는 (C7-C20)페닐 알킬에 의해 치환된 피페리딜 그룹, 또는 피롤리디닐 그룹을 형성한다.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/538,233 US4554276A (en) | 1983-10-03 | 1983-10-03 | 2-Amino-5-hydroxy-4-methylpyrimidine derivatives |
US538233 | 1983-10-03 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR850003402A true KR850003402A (ko) | 1985-06-17 |
KR860001818B1 KR860001818B1 (ko) | 1986-10-24 |
Family
ID=24146051
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019840006093A KR860001818B1 (ko) | 1983-10-03 | 1984-10-02 | 2-아미노-5-하이드록시-4-메틸 피리미딘 유도체의 제조 방법 |
Country Status (25)
Country | Link |
---|---|
US (1) | US4554276A (ko) |
EP (1) | EP0138464B1 (ko) |
JP (1) | JPS6094970A (ko) |
KR (1) | KR860001818B1 (ko) |
AT (1) | ATE47999T1 (ko) |
AU (1) | AU548268B2 (ko) |
CA (1) | CA1215985A (ko) |
DD (1) | DD232698A5 (ko) |
DE (1) | DE3480474D1 (ko) |
DK (1) | DK162222C (ko) |
EG (1) | EG16355A (ko) |
ES (1) | ES8601924A1 (ko) |
FI (1) | FI84479C (ko) |
GR (1) | GR80512B (ko) |
HU (1) | HU194186B (ko) |
IE (1) | IE57633B1 (ko) |
IL (1) | IL73104A (ko) |
NO (1) | NO170883C (ko) |
NZ (1) | NZ209740A (ko) |
PH (1) | PH21038A (ko) |
PL (1) | PL148590B1 (ko) |
PT (1) | PT79278B (ko) |
SU (1) | SU1342417A3 (ko) |
YU (1) | YU44058B (ko) |
ZA (1) | ZA847731B (ko) |
Families Citing this family (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4711888A (en) * | 1985-07-24 | 1987-12-08 | Pfizer Inc. | Hydroxy and alkoxy pyrimidines |
IE58373B1 (en) * | 1986-06-18 | 1993-09-08 | Bloomfield Frederick Jacob | 5-Lipoxygenase pathway inhibitors |
WO1989000423A1 (en) * | 1987-07-09 | 1989-01-26 | Pfizer Inc. | 2-amino-5-hydroxy-4-pyrimidones |
MX14001A (es) * | 1987-12-02 | 1993-06-01 | Pfizer | Procedimiento para preparar derivados de hidroxipirimidinas |
US4910204A (en) * | 1988-06-28 | 1990-03-20 | Pfizer Inc. | 2-amino-5-hydroxy-4-pyrimidones |
DE68910288T2 (de) * | 1988-12-14 | 1994-02-17 | Pfizer | Derivate von 5-Hydroxy- und 5-Methoxy-2-amino-pyrimidin als Inhibitoren der Interleukin-1-Produktion. |
US5071852A (en) * | 1988-12-14 | 1991-12-10 | Pfizer Inc. | Derivatives of 5-hydroxy and 5-methoxy 2-amino-pyrimidines as inhibitors of interleukin-1 production |
US4940712A (en) * | 1989-05-26 | 1990-07-10 | Pfizer Inc. | Derivatives of hydroxyprimidines as leukotriene synthesis inhibitors |
US5204118A (en) * | 1989-11-02 | 1993-04-20 | Mcneil-Ppc, Inc. | Pharmaceutical compositions and methods for treating the symptoms of overindulgence |
US5248682A (en) * | 1991-01-31 | 1993-09-28 | Warner-Lambert Company | 2-substituted-4,6-di-tertiary-butyl-5-hydroxy-1,3-pyrimidines useful as antiinflammatory agents |
US5177079A (en) * | 1991-01-31 | 1993-01-05 | Warner-Lambert Company | 2-substituted-4,6-di-tertiarybutyl-5-hydroxy-1,3-pyrimidines useful as antiinflammatory agents |
US5220025A (en) * | 1992-02-24 | 1993-06-15 | Warner-Lambert Company | 2-substituted amino-4, 6-di-tertiary-butyl-5-hydroxy-1, 3-pyrimidines as antiinflammatory agents |
AU4566093A (en) * | 1992-07-08 | 1994-01-31 | Shell Internationale Research Maatschappij B.V. | Piperidine derivatives |
AU698313B2 (en) * | 1994-03-14 | 1998-10-29 | Government Of The United States Of America, As Represented By The Secretary Of The Department Of Health And Human Services, The | Use of lipoxygenase inhibitors as anti-cancer therapeutic and intervention agents |
US7045519B2 (en) | 1998-06-19 | 2006-05-16 | Chiron Corporation | Inhibitors of glycogen synthase kinase 3 |
ATE274510T1 (de) | 1998-06-19 | 2004-09-15 | Chiron Corp | Glycogen synthase kinase 3 inhibitoren |
SE0000773D0 (sv) * | 2000-03-08 | 2000-03-08 | Astrazeneca Ab | New formulation |
SE0000774D0 (sv) | 2000-03-08 | 2000-03-08 | Astrazeneca Ab | New formulation |
AU2001280445A1 (en) * | 2000-06-23 | 2002-01-08 | Vanderbilt University | Novel chain-breaking antioxidants |
US20020192299A1 (en) * | 2000-12-28 | 2002-12-19 | Rajneesh Taneja | Pharmaceutical compositions of a non-enteric coated proton pump inhibitor with a carbonate salt and bicarbonate salt combination |
US8206741B2 (en) | 2001-06-01 | 2012-06-26 | Pozen Inc. | Pharmaceutical compositions for the coordinated delivery of NSAIDs |
EP2260837A1 (en) * | 2001-06-01 | 2010-12-15 | Pozen, Inc. | Pharmaceutical compositions for the coordinated delivery of NSAIDs |
SE0102993D0 (sv) | 2001-09-07 | 2001-09-07 | Astrazeneca Ab | New self emulsifying drug delivery system |
US20040082618A1 (en) * | 2002-07-03 | 2004-04-29 | Rajneesh Taneja | Liquid dosage forms of acid labile drugs |
US20070243251A1 (en) * | 2002-12-20 | 2007-10-18 | Rajneesh Taneja | Dosage Forms Containing A PPI, NSAID, and Buffer |
US20040121004A1 (en) * | 2002-12-20 | 2004-06-24 | Rajneesh Taneja | Dosage forms containing a PPI, NSAID, and buffer |
WO2004080979A1 (en) * | 2003-03-14 | 2004-09-23 | Lg Life Sciences Ltd. | Novel 3-(2-amino-4-pyrimidinyl)-4-hydroxyphenyl ketone derivatives |
DE102004054080A1 (de) * | 2004-11-09 | 2006-05-11 | Wella Ag | Haut- oder Haarbehandlungsmittel mit Schutzeffekt |
AP2007004047A0 (en) | 2005-01-20 | 2007-06-30 | Pfizer Ltd | Substituted triazole derivatives as oxtocin antagonists |
US9133212B1 (en) | 2005-06-15 | 2015-09-15 | Vanderbilt University | Inhibitors of hemeprotein-catalyzed lipid peroxidation |
US8367669B2 (en) * | 2005-06-15 | 2013-02-05 | Vanderbilt University | Inhibitors of hemeprotein-catalyzed lipid peroxidation |
AU2009204360B2 (en) * | 2008-01-04 | 2014-12-18 | Src, Inc. | The use of analgesic potentiating compounds to potentiate the analgesic properties of an analgesic compound and single dose compositions thereof |
EP2344139A1 (en) | 2008-09-09 | 2011-07-20 | AstraZeneca AB | Method for delivering a pharmaceutical composition to patient in need thereof |
JP2012531409A (ja) | 2009-06-25 | 2012-12-10 | アストラゼネカ・アクチエボラーグ | Nsaid関連潰瘍を発症するリスクがある患者の処置方法 |
EA028049B1 (ru) | 2011-12-28 | 2017-10-31 | Поузен Инк. | Улучшенные композиции и способы доставки омепразола и ацетилсалициловой кислоты |
US11324727B2 (en) | 2020-07-15 | 2022-05-10 | Schabar Research Associates, Llc | Unit oral dose compositions composed of naproxen sodium and famotidine for the treatment of acute pain and the reduction of the severity of heartburn and/or the risk of heartburn |
IL299845A (en) | 2020-07-15 | 2023-03-01 | Schabar Res Associates Llc | Oral unit dose compounds consisting of ibuprofen and famotidine for the treatment of acute pain and to reduce the severity and/or risk of heartburn |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4000138A (en) * | 1966-03-31 | 1976-12-28 | Imperial Chemical Industries Limited | Organic compounds and compositions containing them |
US3932617A (en) * | 1974-05-24 | 1976-01-13 | The Upjohn Company | Interferon induction |
DE2814984A1 (de) * | 1978-04-07 | 1979-10-18 | Bayer Ag | Pyrimidin(5)yl-(thiono)(thiol)- phosphor(phosphon)-saeureester bzw. -esteramide, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide |
IN153791B (ko) * | 1979-03-10 | 1984-08-18 | Soc D Etudes Prod Chimique | |
US4416885A (en) * | 1979-11-02 | 1983-11-22 | Huve Pierre M | Use of isopropylaminopyrimidine in the chemotherapy of muscular dystrophy, myopathy and myotonia |
OA07362A (fr) * | 1980-10-27 | 1984-06-30 | May & Baker Ltd | Dérivés de la pyrimidine, leur procédé de préparation et les compositions les contenant. |
US4435396A (en) * | 1982-05-10 | 1984-03-06 | Pfizer Inc. | Antiulcer 2-guanidino-4-(2-substituted-amino-4-imidazolyl)thiazoles and process therefor |
-
1983
- 1983-10-03 US US06/538,233 patent/US4554276A/en not_active Expired - Fee Related
-
1984
- 1984-09-26 IL IL73104A patent/IL73104A/xx unknown
- 1984-09-27 EP EP84306575A patent/EP0138464B1/en not_active Expired
- 1984-09-27 DE DE8484306575T patent/DE3480474D1/de not_active Expired
- 1984-09-27 AT AT84306575T patent/ATE47999T1/de not_active IP Right Cessation
- 1984-09-28 PT PT79278A patent/PT79278B/pt not_active IP Right Cessation
- 1984-10-01 PH PH31288A patent/PH21038A/en unknown
- 1984-10-01 IE IE2494/84A patent/IE57633B1/en not_active IP Right Cessation
- 1984-10-01 DD DD84267874A patent/DD232698A5/de not_active IP Right Cessation
- 1984-10-01 CA CA000464388A patent/CA1215985A/en not_active Expired
- 1984-10-01 GR GR80512A patent/GR80512B/el unknown
- 1984-10-02 NZ NZ209740A patent/NZ209740A/en unknown
- 1984-10-02 YU YU1695/84A patent/YU44058B/xx unknown
- 1984-10-02 ZA ZA847731A patent/ZA847731B/xx unknown
- 1984-10-02 PL PL1984249833A patent/PL148590B1/pl unknown
- 1984-10-02 HU HU843731A patent/HU194186B/hu not_active IP Right Cessation
- 1984-10-02 KR KR1019840006093A patent/KR860001818B1/ko not_active IP Right Cessation
- 1984-10-02 SU SU843796139A patent/SU1342417A3/ru active
- 1984-10-02 FI FI843864A patent/FI84479C/fi not_active IP Right Cessation
- 1984-10-02 NO NO843968A patent/NO170883C/no unknown
- 1984-10-02 AU AU33768/84A patent/AU548268B2/en not_active Ceased
- 1984-10-02 DK DK472184A patent/DK162222C/da not_active IP Right Cessation
- 1984-10-03 ES ES536499A patent/ES8601924A1/es not_active Expired
- 1984-10-03 JP JP59207904A patent/JPS6094970A/ja active Granted
- 1984-10-03 EG EG616/84A patent/EG16355A/xx active
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