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HUP0500109A3 - Synthesis of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones - Google Patents

Synthesis of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones

Info

Publication number
HUP0500109A3
HUP0500109A3 HU0500109A HUP0500109A HUP0500109A3 HU P0500109 A3 HUP0500109 A3 HU P0500109A3 HU 0500109 A HU0500109 A HU 0500109A HU P0500109 A HUP0500109 A HU P0500109A HU P0500109 A3 HUP0500109 A3 HU P0500109A3
Authority
HU
Hungary
Prior art keywords
pyrid
pyrazolo
dihydro
ones
synthesis
Prior art date
Application number
HU0500109A
Other languages
English (en)
Original Assignee
Bristol Myers Squibb Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of HUP0500109A2 publication Critical patent/HUP0500109A2/hu
Publication of HUP0500109A3 publication Critical patent/HUP0500109A3/hu

Links

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
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two 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
    • C07D211/86—Oxygen atoms
    • C07D211/88—Oxygen atoms attached in positions 2 and 6, e.g. glutarimide
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two 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
    • C07D211/86—Oxygen atoms
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
HU0500109A 2001-12-10 2002-12-03 Synthesis of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones HUP0500109A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US33908501P 2001-12-10 2001-12-10
PCT/US2002/038559 WO2003049681A2 (en) 2001-12-10 2002-12-03 Synthesis of 4,5-dihydro-pyrazolo [3,4-c] pyrid-2-ones

Publications (2)

Publication Number Publication Date
HUP0500109A2 HUP0500109A2 (hu) 2005-05-30
HUP0500109A3 true HUP0500109A3 (en) 2007-08-28

Family

ID=23327425

Family Applications (1)

Application Number Title Priority Date Filing Date
HU0500109A HUP0500109A3 (en) 2001-12-10 2002-12-03 Synthesis of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones

Country Status (13)

Country Link
US (3) US6919451B2 (hu)
EP (1) EP1467984A4 (hu)
JP (1) JP2005511712A (hu)
KR (1) KR20040073467A (hu)
CN (1) CN1639147A (hu)
AU (1) AU2002346624A1 (hu)
BR (1) BR0214845A (hu)
HU (1) HUP0500109A3 (hu)
IL (1) IL161955A0 (hu)
MX (1) MXPA04005508A (hu)
PL (1) PL371930A1 (hu)
TW (2) TW200738672A (hu)
WO (1) WO2003049681A2 (hu)

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TWI320039B (en) 2001-09-21 2010-02-01 Lactam-containing compounds and derivatives thereof as factor xa inhibitors
US7396932B2 (en) 2004-09-28 2008-07-08 Bristol-Myers Squibb Company Process for preparing 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones
US20070203178A1 (en) * 2004-09-28 2007-08-30 Malley Mary F Crystalline solvates of apixaban
CN101065379B (zh) * 2004-09-28 2011-05-11 布里斯托尔-迈尔斯斯奎布公司 制备4,5-二氢-吡唑并[3,4-c]吡啶-2-酮的方法
US20060069085A1 (en) * 2004-09-28 2006-03-30 Rulin Zhao Preparation of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones
US7304157B2 (en) 2004-09-28 2007-12-04 Bristol-Myers Squibb Company Efficient synthesis of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones
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CN103626759B (zh) * 2012-08-24 2015-10-21 上海医药工业研究院 一种阿哌沙班的中间体的制备方法
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CZ2013305A3 (cs) 2013-04-23 2014-11-05 Zentiva, K.S. Nové krystalické formy APIXABANU a způsob jejich přípravy
US20160113912A1 (en) 2013-06-18 2016-04-28 Cadila Healthcare Limited An improved process for the preparation of apixaban and intermediates thereof
CN103739541B (zh) * 2014-01-07 2016-01-20 上海现代制药股份有限公司 5,6-二氢-3-(4-吗啉基)-1-[4-(2-氧代-1-哌啶基)苯基]-2(1h)-吡啶酮的制备方法
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CN103896940B (zh) * 2014-03-25 2016-02-03 江苏弘和药物研发有限公司 一种阿哌沙班的合成方法
CN103923080B (zh) * 2014-04-04 2016-06-22 苏州景泓生物技术有限公司 一种制备抗血栓药物阿哌沙班的方法
CN104045637B (zh) * 2014-04-18 2016-04-06 河北科技大学 一种阿哌沙班的制备方法
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CN104277037B (zh) * 2014-09-19 2015-12-09 广东东阳光药业有限公司 含有螺环的吡唑并哌啶酮类化合物及其组合物及用途
CN104327074B (zh) * 2014-09-19 2016-01-06 广东东阳光药业有限公司 含有内酰胺取代基的吡唑并哌啶酮类化合物及其组合物及用途
CN104311558B (zh) * 2014-09-19 2016-06-01 广东东阳光药业有限公司 含有环己烷取代基的吡唑并哌啶酮类化合物及其组合物及用途
CN104277040B (zh) * 2014-09-19 2016-04-20 广东东阳光药业有限公司 含有酰基哌嗪酮取代基的吡唑并哌啶酮类化合物及其组合物及用途
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EP3212620B1 (en) * 2014-10-28 2020-11-25 Jubilant Generics Limited (Formerly Jubilant Life Sciences Division) Process for the preparation of apixaban and intermediates thereof
HU230991B1 (hu) * 2014-11-19 2019-08-28 Egis Gyógyszergyár Zrt. Eljárás és köztitermék apixaban előállítására
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CN104892601B (zh) * 2015-06-09 2017-09-19 江苏中邦制药有限公司 一种抗血栓药物阿哌沙班的制备方法
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CN106632312B (zh) * 2015-11-03 2019-05-14 上海医药工业研究院 一种阿哌沙班有关物质、中间体、制备方法及其应用
CN105732618A (zh) * 2016-02-02 2016-07-06 扬州大学 一种合成4-(2-氧代哌啶-1-基)芳基羧酸乙酯类化合物的方法
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CN106117200B (zh) * 2016-06-27 2018-02-02 张士伟 预防或治疗关节置换静脉血栓药物阿哌沙班的制备方法
CN115819417A (zh) 2016-09-09 2023-03-21 因赛特公司 作为hpk1调节剂的吡唑并吡啶衍生物及其用于治疗癌症的用途
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CN107434806A (zh) * 2016-12-09 2017-12-05 陕西科技大学 一种阿哌沙班羧酸衍生物的γ晶型固体物质及其制备方法与用途
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CN107955003A (zh) * 2017-12-28 2018-04-24 河北常山生化药业股份有限公司 一种阿哌沙班中间体2合成过程中特定杂质s4的清除方法
CN107936015B (zh) * 2017-12-28 2020-05-12 浙江天宇药业股份有限公司 一种n-1晶型的阿哌沙班的合成方法
US10745388B2 (en) 2018-02-20 2020-08-18 Incyte Corporation Indazole compounds and uses thereof
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WO2019164847A1 (en) 2018-02-20 2019-08-29 Incyte Corporation Indazole compounds and uses thereof
US11299473B2 (en) 2018-04-13 2022-04-12 Incyte Corporation Benzimidazole and indole compounds and uses thereof
US10899755B2 (en) 2018-08-08 2021-01-26 Incyte Corporation Benzothiazole compounds and uses thereof
ES2973117T3 (es) 2018-09-25 2024-06-18 Incyte Corp Compuestos de pirazolo[4,3-d]pirimidina como moduladores de ALK2 y/o FGFR
KR102188341B1 (ko) * 2018-10-24 2020-12-08 하나제약 주식회사 아픽사반의 제조방법
JP2022543155A (ja) 2019-08-06 2022-10-07 インサイト・コーポレイション Ｈｐｋ１阻害剤の固体形態
CN111253392B (zh) * 2019-12-17 2021-06-11 哈尔滨珍宝制药有限公司 一种制备阿哌沙班的方法
CN113214142B (zh) * 2020-01-21 2024-01-30 浙江九洲药业股份有限公司 一种阿哌沙班的中间体及制备方法
JP2022022550A (ja) * 2020-06-26 2022-02-07 ダイト株式会社 アピキサバンの新規製造方法
CN112142736B (zh) * 2020-10-29 2021-08-10 怀化学院 一种阿哌沙班杂质1的制备方法

Family Cites Families (8)

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Publication number Priority date Publication date Assignee Title
FR2459240A1 (fr) * 1979-06-21 1981-01-09 Cm Ind Aminopiperidines anorexigenes, procede pour leur preparation, intermediaires dans ledit procede et medicaments qui les contiennent
EP1140941B1 (en) 1998-12-23 2004-10-20 Bristol-Myers Squibb Pharma Company Nitrogen containing heterobicycles as factor xa inhibitors
US6329527B1 (en) 1999-10-21 2001-12-11 Bristol-Myers Squibb Pharma Company Synthesis of 1,3,5-trisubstituted pyrazoles
TWI320039B (en) 2001-09-21 2010-02-01 Lactam-containing compounds and derivatives thereof as factor xa inhibitors
PL204263B1 (pl) 2001-09-21 2009-12-31 Bristol Myers Squibb Co Pochodna 1H-pirazolo[3,4-c]pirydyny i jej zastosowanie oraz kompozycja farmaceutyczna i jej zastosowanie
US7396932B2 (en) * 2004-09-28 2008-07-08 Bristol-Myers Squibb Company Process for preparing 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones
US20060069085A1 (en) * 2004-09-28 2006-03-30 Rulin Zhao Preparation of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones
US7304157B2 (en) * 2004-09-28 2007-12-04 Bristol-Myers Squibb Company Efficient synthesis of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones

Also Published As

Publication number Publication date
BR0214845A (pt) 2004-12-07
JP2005511712A (ja) 2005-04-28
MXPA04005508A (es) 2004-12-06
PL371930A1 (en) 2005-07-11
CN1639147A (zh) 2005-07-13
US20070027186A1 (en) 2007-02-01
EP1467984A2 (en) 2004-10-20
IL161955A0 (en) 2005-11-20
US20030181466A1 (en) 2003-09-25
EP1467984A4 (en) 2005-12-07
US20050245566A1 (en) 2005-11-03
US6919451B2 (en) 2005-07-19
WO2003049681A3 (en) 2003-09-18
KR20040073467A (ko) 2004-08-19
TW200738672A (en) 2007-10-16
WO2003049681A2 (en) 2003-06-19
HUP0500109A2 (hu) 2005-05-30
TW200303201A (en) 2003-09-01
US7153960B2 (en) 2006-12-26
AU2002346624A1 (en) 2003-06-23

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