LV11971B - Pirolidīnhidroksāmskābes atvasinājumi un to iegūšanas paņēmiens - Google Patents

Pirolidīnhidroksāmskābes atvasinājumi un to iegūšanas paņēmiens Download PDF

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LV11971B
LV11971B LVP-97-203A LV970203A LV11971B LV 11971 B LV11971 B LV 11971B LV 970203 A LV970203 A LV 970203A LV 11971 B LV11971 B LV 11971B
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hydroxy
phenyl
acetamide
hydrogen
compound
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Fumitaka Ito
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Pfizer Inc
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Claims (13)

1LV 11971 Izgudrojuma formula 1. Savienojums ar formulu (I), Ar
A ir ūdeņraža atoms, hidroksilgrupa vai OY, kur Y ir hidroksilgrupas aiz-sarggrupa; Ar ir fenilgrupa, kas neobligāti aizvietota ar vienu vai vairākiem aizvietotājiem no rindas: halogēna atoms, hidroksilgrupa, Ci^alkilgrupa, Ci^alk-oksigrupa, trifluormetilgrupa, Ci^alkoksi-Ci^alkoksigrupa un karboksil-aizvietota Ci^alkoksigrupa; X ir fenilgrupa, naftilgrupa, bifenilgrupa, indanilgrupa, benzofuranilgrupa, benzotienilgrupa, 1-oksotetralin-6-iigrupa, Ci-*alkilendioksigrupa, piri-dinilgrupa, furanilgrupa vai tienilgrupa, pie kam minētas grupas neobligāti aizvietotas ar 1 - 3 aizvietotājiem no rindas: halogēna atoms, Ci^alkilgrupa, Ci^alkoksigrupa, hidroksilgrupa, nitrogrupa, trifluormetilgrupa un metilsulfonilgrupa; R ir ūdeņraža atoms, Ci^alkilgrupa vai hidroksilgrupas aizsarggrupa, kā arī minētā savienojuma sālis.
2. Savienojums pēc 1. punkta, kurā A ir ūdeņraža atoms vai hidroksilgrupa; R ir ūdeņraža atoms vai C-Malkilgrupa.
3. Savienojums pēc 2. punkta, kurā Ar ir fenilgrupa. 2
4. Savienojums pēc 3. punkta, kurā X ir fenilgrupa, kas aizvietota ar 1 - 3 aizvietotājiem no rindas: hlora atoms, metilgrupa un trifluormetilgrupa; R ir ūdeņraža atoms.
5. Savienojums pēc 4. punkta, kurā X ir 3,4-dihlorfenilgrupa.
6. Savienojums pēc 4. punkta, kas ņemts no rindas: 2-(3,4-dihlorfenil)-N-hidroksi-N-[1-(S)-fenil-2-(1-pirolidinil)etilļacetamTds; 2-(2,3,6-trihlorfenil)-N-hidroksi-N-[1-(S)-fenil-2-(1-pirolidinil)etil]acetamTds; 2-(4-trifluormetilfenil)-N-hidroksi-N-[1-(S)-fenil-2-(1-pirolidinil)etiljacetamīds; 2-(2,4,6-trimetilfenil)-N-hidroksi-N-[1-(S)-fenil-2-(1-pirolidinil)etilļacetamīds; 2-(3,4-dihlorfenil)-N-hidroksi-N-[2-(3-(S)-hidroksipirolidin-1-il)-1-(S)-feni!etii]- acetamīds; 2-{4-bromfenil)-N-hidroksi-N-[2-(3-(S)-hidroksipirolidin-1-il)-1-(S)-feniletil]- acetamīds; 2-(4-trifluormetilfenil)-N-hidroksi-N-[2-(3-(S)-hidroksipirolidin-1-il)-1-(S)-feniletil]- acetamīds; 2-(4-hlorfenil)-N-hidroksi-N-[2-(3-(S)-hidroksipirolidin-1-il)-1-(S)-feniletilj- acetamīds; 2-(2,3-dihlorfenil)-N-hidroksi-N-[2-(3-(S)-hidroksipirolidin-1-il)-1-(S)-feniletil]- acetamīds; 2-(2,4-dihlorfenil)-N-hidroksi-N-[2-(3-(S)-hidroksipirolidin-1-il)-1-(S)-feniletil]- acetamTds; 2-(2,5-dihlorfenil)-N-hidroksi-N-[2-(3-(S)-hidroksipirolidin-1-il)-1-(S)-feniletil]- acetamīds; 2-(2,6-dihlorfenil)-N-hidroksi-N-[2-(3-(S)-hidroksipirolidin-1-il)-1-(S)-feniletilļ- acetamīds; 2-(2,3,6-trihlorfenil)-N-hidroksi-N-[2-(3-(S)-hidroksipirolidin-1-il)-1-(S)-feniletil]- acetamīds; 2-(3,4-dihlorfenil)-N-[2-(3-(S)-hidroksipirolidin-1-il)-1-(S)-feniletil]-acetamīds; 2-(3,4-dimetilfenil)-N-hidroksi-N-[2-(3-(S)-hidroksipirolidin-1-il)-1-(S)-feniletil]- acetamTds. 3 LV 11971
7. Savienojums pēc 1. punkta, kurā A ir OY un R ir hidroksilgrupas aizsarggrupa no rindas: benzilgrupa, trifenilmetilgrupa, tetrahidropiranilgrupa, metoksimetilgrupa un R1R2R3Si- grupa, kur katrs no R1, R2 un Rs ir Ci^alkil-grupa vai fenilgrupa.
8. Farmaceitiskā kompozīcija, kas satur savienojumu pēc 1. punkta un farmaceitiski inertu nesēju, un kas pielietojama kā analgētisks, pretiekaisuma, diurētisks, anestētisks, neiroprotektīvs līdzeklis, līdzeklis triekas ārstēšanai vai līdzeklis tādu funkcionālu zarnu slimību kā vēdersāpju ārstēšanai.
9. Savienojuma pēc 1. punkta pielietojums tādu ārstniecības līdzekļu ražošanai, kas paredzēti tādu zīdītājus slimību ārstēšanai, kurās nepieciešams kapa-receptora agonists.
10. Savienojums ar formulu (II), Ar
kurā: A ir ūdeņraža atoms, hidroksilgrupa vai OY, kur Y ir hidroksilgrupas aizsarggrupa Ar ir fenilgrupa, neobligāti aizvietota ar vienu vai vairākiem aizvietotājiem no rindas: halogēna atoms, hidroksilgrupa, Ci^alkilgrupa, Ci^alkoksi-grupa, trifluormetilgrupa, Ci^alkoksi-Ci^alkoksigrupa un karboksilaizvie-tota C-Malkoksigrupa; R ir ūdeņraža atoms, Ci^alkilgrupa vai hidroksilgrupas aizsarggrupa.
11. Paņēmiens savienojuma ar formulu (II) iegūšanai, kas ietver etanolamīna (III) reakciju ar hidroksilamīna atvasinājumu (IV),
(V) 4 kuru tālāk apstrādā ar metānsulfonilhlorīdu bāzes klātbūtnē, un pēc tam pievieno aizsargātu hidroksilamīnu, noslēgumā, ja nepieciešams, nošķeļot aizsarggrupu.
12. Paņēmiens savienojuma ar formulu (II) iegūšanai, kas ietver pirolidTna ar formulu (VII) apstrādi ar aizvietotu vai neaizvietotu feniloksirānu (VIII),
O (vil) (vm) veidojot savienojumu (IX) un (X) maisījumu,
kuru apstrādā ar metānsulfonilhlorīdu bāzes klātbūtnē un pievieno aizsargātu hidroksilamīnu, noslēgumā, ja nepieciešams, nošķeļot aizsarggrupu.
13. Paņēmiens savienojuma ar formulu (I) iegūšanai, kas ietver savienojuma ar formulu (II), kurā R ir hidroksilgrupas aizsarggrupa, apstrādi ar karbonskābi XCH2COOH, aizsarggrupas atšķelšanu, un, ja nepieciešams, iegūtā savienojuma alkilēšanu.
LVP-97-203A 1995-03-31 1997-10-21 Pirolidīnhidroksāmskābes atvasinājumi un to iegūšanas paņēmiens LV11971B (lv)

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JP9500631 1995-03-31
PCT/JP1996/000820 WO1996030339A1 (en) 1995-03-31 1996-03-28 Pyrrolidinyl hydroxamic acid compounds and their production process

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TNSN97092A1 (ar) 1996-09-18 1999-12-31 Agouron Pharma مثبطات انزيم بروتيني فلزي وتركيبات صيدلانية تحتوي على تلك المثبتطات واستخدامها الصيدلاني وطرق ومركبات وسيطة مفيدة لتحضير التركيبات المذكورة.
DE69720518T2 (de) * 1996-12-02 2004-02-26 Kyorin Pharmaceutical Co., Ltd. Neue derivate von n-substituierten pyrrolidin derivaten und deren herstellungsverfahren
WO1998030540A1 (en) * 1997-01-10 1998-07-16 Merck & Co., Inc. Efficient synthesis of a chiral mediator
EP0982297A3 (en) * 1998-08-24 2001-08-01 Pfizer Products Inc. Process for the preparation of hydroxy-pyrrolidinyl hydroxamic acid derivatives being opioid kappa receptor agonists
KR100295740B1 (ko) * 1998-09-17 2001-11-05 박영구 N-치환된-하이드록시고리화알킬아민유도체의제조방법
US6444829B1 (en) * 2000-07-19 2002-09-03 Hoffmann-La Roche Inc. Pyrrolidine compounds
JP2005508851A (ja) 2001-04-30 2005-04-07 ファイザー・プロダクツ・インク カッパーアゴニストとして有用なヒドロキシピロリジニルエチルアミン化合物の調製方法
US7091357B2 (en) * 2001-12-26 2006-08-15 University Of Kentucky Research Foundation Chain-modified pyridino-N substituted nicotine compounds for use in the treatment of CNS pathologies
WO2004039785A1 (en) * 2002-11-01 2004-05-13 Pfizer Products Inc. Process for the preparation of pyrrolidinyl ethylamine compounds via a copper-mediated aryl amination
GB0821010D0 (en) * 2008-11-17 2008-12-24 Univ Warwick Plant development control composition
WO2012155199A1 (en) 2011-05-16 2012-11-22 Bionomics Limited Amine derivatives as potassium channel blockers
KR101773331B1 (ko) * 2012-03-05 2017-08-31 닥터 레디스 레보러터리즈 리미티드 카파 오피오이드 수용체(κor) 작용제인 치환된 헤테로시클릭 아세트아미드
GB201210395D0 (en) * 2012-06-11 2012-07-25 Syngenta Participations Ag Crop enhancement compositions

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AU5121196A (en) 1996-10-16
SI9620039A (sl) 1998-08-31
DE69626009D1 (de) 2003-03-06
NO974513D0 (no) 1997-09-29
CA2213815C (en) 2001-12-18
HUP9900767A2 (hu) 1999-07-28
MX9707454A (es) 1998-07-31
NO974513L (no) 1997-09-29
EP0817772A1 (en) 1998-01-14
AR002729A1 (es) 1998-04-29
TNSN96045A1 (fr) 2005-03-15
US5952369A (en) 1999-09-14
IS4547A (is) 1997-08-19
IL129479A0 (en) 2000-02-29
LV11971A (lv) 1998-02-20
CZ306497A3 (cs) 1998-07-15
YU18696A (sh) 1999-06-15
US6110947A (en) 2000-08-29
AP625A (en) 1997-12-24
DK0817772T3 (da) 2003-05-19
ATE231840T1 (de) 2003-02-15
IL117440A0 (en) 1996-07-23
KR100258657B1 (ko) 2000-07-01
AU693336B2 (en) 1998-06-25
OA10518A (en) 2002-04-22

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