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(7R,9aS)-2-BOC-7-(5-fluoroindol-1-yl)methyl-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazine | 178931-23-2

中文名称
——
中文别名
——
英文名称
(7R,9aS)-2-BOC-7-(5-fluoroindol-1-yl)methyl-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazine
英文别名
tert-butyl (7R,9aS)-7-[(5-fluoroindol-1-yl)methyl]-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazine-2-carboxylate
(7R,9aS)-2-BOC-7-(5-fluoroindol-1-yl)methyl-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazine化学式
CAS
178931-23-2
化学式
C22H30FN3O2
mdl
——
分子量
387.498
InChiKey
JRGJUIHWKAUIQX-APWZRJJASA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    28
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.59
  • 拓扑面积:
    37.7
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (7R,9aS)-2-BOC-7-(5-fluoroindol-1-yl)methyl-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazine三氟乙酸 为溶剂, 以2.0 g (90%)的产率得到(7R,9AS)-7-(5-fluoroindol-1-yl)methyl-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazine
    参考文献:
    名称:
    2,7-substituted octahydro-1H-pyrido\x9b1,2-a!pyrazine derivatives
    摘要:
    通用公式I中的取代吡啶并噻唑的化合物,其中Ar和Ar.sup.1代表各种碳环和杂环芳香环;A代表O、S、SO、SO.sub.2、C.dbd.O、CHOH,或--(CR.sup.3 R.sup.4),n为0-2,以及它们的前体是体内多巴胺受体亚型的配体,因此在治疗多巴胺系统疾病中很有用。
    公开号:
    US05852031A1
  • 作为产物:
    描述:
    5-氟吲哚(7R,9aS)-2-BOC-7-(methanesulfonyloxy)methyl-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazineN,N-二甲基甲酰胺 为溶剂, 以3.09 g (36%)的产率得到(7R,9aS)-2-BOC-7-(5-fluoroindol-1-yl)methyl-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazine
    参考文献:
    名称:
    2,7-substituted octahydro-1H-pyrido\x9b1,2-a!pyrazine derivatives
    摘要:
    通用公式I中的取代吡啶并噻唑的化合物,其中Ar和Ar.sup.1代表各种碳环和杂环芳香环;A代表O、S、SO、SO.sub.2、C.dbd.O、CHOH,或--(CR.sup.3 R.sup.4),n为0-2,以及它们的前体是体内多巴胺受体亚型的配体,因此在治疗多巴胺系统疾病中很有用。
    公开号:
    US05852031A1
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文献信息

  • 2,7-Substituted octahydro-1H-pyrido[1,2-a]pyrazine derivatives as ligands for serotonin receptors
    申请人:——
    公开号:US20040214830A1
    公开(公告)日:2004-10-28
    Substituted pyrido[1,2-a]pyrazines of general formula I; wherein Ar and Ar 1 represent various carbocyclic and heterocyclic aromatic rings; A represents O, S, SO, SO 2 , CHOH, C═O, or —(CR 3 R 4 ); and n is 0-2, as well as precursors thereto, are ligands for dopamine receptor subtypes and serotonin (5HT) within the body and are therefore useful in the treatment of disorders of the dopamine and serotonin systems: 1
    通式I的取代吡啶[1,2-a]吡嗪,其中Ar和Ar1代表各种碳环和杂环芳香环;A代表O,S,SO,SO2,CHOH,C═O或—(CR3R4);n为0-2,以及其前体,是体内多巴胺受体亚型和5-羟色胺(5HT)的配体,因此在治疗多巴胺和5-羟色胺系统紊乱方面有用:1
  • 2,7-substituted octahydro-1H-pyrido[1,2-A]pyrazine derivatives as ligands for serotonin receptors
    申请人:Pfizer Inc.
    公开号:US20030055061A1
    公开(公告)日:2003-03-20
    Substituted pyrido[1,2-a]pyrazines of general formula I; wherein Ar and Ar 1 represent various carbocyclic and heterocyclic aromatic rings; A represents O, S, SO, SO 2 , CHOH, C═O, or —(CR 3 R 4 ); and n is 0-2, as well as precursors thereto, are ligands for dopamine receptor subtypes and serotonin (5HT) within the body and are therefore useful in the treatment of disorders of the dopamine and serotonin systems: 1
    通式为I的取代的吡啶并[1,2-a]吡嗪,其中Ar和Ar1代表各种碳环和杂环芳香环;A代表O,S,SO,SO2,CHOH,C═O或—(CR3R4);n为0-2,以及其前体,是体内多巴胺受体亚型和血清素(5HT)的配体,因此在治疗多巴胺和血清素系统的疾病方面具有用处。
  • 2,7-substituted octahydro-1H-pyrido[1,2-A]pyrazine derivatives as ligands for serotonin receptors
    申请人:Pfizer Inc
    公开号:US06231833B1
    公开(公告)日:2001-05-15
    Substituted pyrido[1,2-a]pyrazines of general formula I; wherein Ar and Ar1 represent various carbocyclic and heterocyclic aromatic rings; A represents O, S, SO, SO2, CHOH, C═O, or —(CR3R4); and n is 0-2, as well as precursors thereto, are ligands for dopamine receptor subtypes and serotonin (5HT) within the body and are therefore useful in the treatment of disorders of the dopamine and serotonin systems:
    通式为I的取代的吡啶并[1,2-a]吡嗪化合物;其中Ar和Ar1代表不同的碳环和杂环芳香环;A代表O、S、SO、SO2、CHOH、C═O或—(CR3R4);n为0-2,以及其前体,是体内多巴胺受体亚型和血清素(5HT)的配体,因此在治疗多巴胺和血清素系统疾病方面有用。
  • 2,7-substituted octahydro-1H-pyrido[1,2-a]pyrazine derivatives as ligands for serotonin receptors
    申请人:Pfizer Inc.
    公开号:US07220753B2
    公开(公告)日:2007-05-22
    Substituted pyrido[1,2-a]pyrazines of general formula I; wherein Ar and Ar1 represent various carbocyclic and heterocyclic aromatic rings; A represents O, S, SO, SO2, CHOH, C═O, or —(CR3R4); and n is 0–2, as well as precursors thereto, are ligands for dopamine receptor subtypes and serotonin (5HT) within the body and are therefore useful in the treatment of disorders of the dopamine and serotonin systems:
    通式为I的取代的吡啶并[1,2-a]吡嗪化合物;其中Ar和Ar1代表不同的碳环和杂环芳香环;A代表O,S,SO,SO2,CHOH,C═O或—(CR3R4);n为0-2,以及其前体,是体内多巴胺受体亚型和5-羟色胺(5HT)的配体,因此在治疗多巴胺和5-羟色胺系统紊乱方面非常有用。
  • 2,7-Substituted octahydro-1H-pyrido (1,2-A)pyrazine derivatives as ligands for serotonin receptors
    申请人:Pfizer Products Inc.
    公开号:EP1074257A1
    公开(公告)日:2001-02-07
    Substituted pyrido[1,2-a]pyrazines of general formula I; wherein Ar and Ar1 represent various carbocyclic and heterocyclic aromatic rings; A represents O, S, SO, SO2, CHOH, C=O, or -(CR3R4); and n is 0-2, as well as precursors thereto, are ligands for dopamine receptor subtypes and serotonin (5HT) within the body and are therefore useful in the treatment of disorders of the dopamine and serotonin systems:
    通式 I 的取代吡啶并[1,2-a]吡嗪;其中 Ar 和 Ar1 代表各种碳环和杂环芳香环;A 代表 O、S、SO、SO2、CHOH、C=O 或-(CR3R4);n 为 0-2,及其前体是体内多巴胺受体亚型和血清素(5HT)的配体,因此可用于治疗多巴胺和血清素系统疾病:
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同类化合物

麦可弗汀A 六氢-2-甲基-2H-吡啶并[1,2-a]吡嗪-1,6-二酮 八氢吡啶并〔1,2-A〕吡嗪-6-酮 八氢吡啶并[1,2-a]吡嗪 八氢-吡啶并[1,2-A]吡嗪-4-酮盐酸盐 八氢-3-甲基-2H-吡啶并[1,2-a]吡嗪 八氢-2H-吡啶并[1,2-a]吡嗪-6-甲醇 7-甲氧基辛a氢-2H-吡啶并[1,2-a]吡嗪-2-胺 7-乙基八氢-2H-吡啶并[1,2-a]吡嗪-2-胺 6-甲基八氢-2H-吡啶并[1,2-a]吡嗪-2-胺 4H-吡唑[1,2-A]吡嗪-4-八氢酮 3-甲基八氢-2H-吡啶并[1,2-a]吡嗪-2-胺 2-苄基八氢-1H-吡啶并[1,2-a]吡嗪 2-硝基八氢-2H-吡啶并[1,2-a]吡嗪 2-乙基六氢-2H-吡啶并[1,2-a]吡嗪-1(6H)-酮 2-(9-甲基-3,9-二氮杂双环[3.3.1]壬-3-基)乙胺 2-(4-甲硫基唑-5-基)乙基丁酸酯 2,3,4,6,7,8,9,9alpha-八氢-1H-吡啶并[1,2-a]吡嗪-3-基甲醇 1,1'-联苯基,2-乙基-5-甲氧基- (R)-八氢吡啶并[1,2-A〕吡嗪二盐酸盐 (9aS)-八氢-4H-吡啶并[1,2-a]吡嗪-4-酮 (9aR)-八氢-2H-吡啶并[1,2-a]吡嗪 (9SS)-八氢-2-吡啶-吡嗪盐酸盐[1,2-A] (7r,9as)-八氢-2H-吡啶并[1,2-a]吡嗪-7-甲醇 (3S,6S)-3-苄基-1,4-二氮杂双环[4.4.0]癸烷-2,5-二酮 ((7S,9as)-八氢-1H-吡啶并[1,2-a]吡嗪-7-基)甲醇 ((6R,9as)-八氢-1H-吡啶并[1,2-a]吡嗪-6-基)甲醇 (S)-octahydro-2H-pyrido[1,2-a]pyrazine dihydrochloride (7R,9AS)-trans-(2,5-Difluoro-phenyl)-[7-(3-pyrrolidin-1-ylmethyl-phenoxymethyl)-octahydro-pyrido[1,2-a]pyrazin-2-yl]-methanone oxime (7RS,9ASR)-7-hydroxymethyl-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazine (6aα,10aα,11aα)-1,3,4,6,6a,7,8,9,10,10a,11,11a-Dodecahydro-2H-pyrazino-[1,2-b]isoquinoline-1,3-dione 17-β-cyanomarcfortine A 17-α-cyanomarcfortine A marcfortine A (trans)-benzyl 7-(8-chloroimidazo[1,5-a]pyrazin-3-yl)-4-oxohexahydro-1H-pyrido[1,2-a]pyrazine-2(6H)-carboxylate 3,5-dibromo-N-{(2S)-2-(4-fluorophenyl)-4-[3-(octahydro-2H-pyrido[1,2-a]pyrazin-2-yl)-azetidin-1-yl]butyl}-N-methylbenzamide acetate 2H-Pyrido[1,2-a]pyrazine, 2-[1-(3-fluorophenyl)ethyl]octahydro-3-methyl- 3-(4-octahydro-2H-pyrido[1,2-a]pyrazin-2-ylbutoxy)benzonitrile 1-[(7R,9aS)-2-BOC-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazin-7-ylmethyl]-1,3-dihydro-indol-2-one 2-<2-(3-indolyl)ethyl>-3-hydroxy-1-oxo-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido<1.2-a>pyrazine 2-<2-(3-indolyl)ethyl>-1-hydroxy-3-oxo-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido<1.2-a>pyrazine (1R,3R)-11,14-Dihydroxy-16-(hydroxymethyl)-13-methoxy-12,20-dimethyl-5-oxa-8,17,20-triazahexacyclo[15.3.1.03,19.04,8.09,18.010,15]henicosa-10(15),11,13-triene-21-carbonitrile trans-perhydrodiazaphenanthrene cis-perhydrodiazaphenanthrene tert-butyl (1aR,4S,6aR,7aR)-4-{[(1S,2S)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]carbamoyl}octahydro-5H-cyclopropa[4,5]pyrrolo[1,2-a]pyrazine-5-carboxylate 2-benzyl-hexahydro-6H-pyrido[1,2-a]pyrazine-1,4-dione (7R,9aS)-2-BOC-7-(4-fluorophenoxy)methyl-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazine trans-7-(3-piperidin-1-ylpropoxymethyl)-octahydro-pyrido[1,2-a]pyrazine-2-carboxylic acid tert-butyl ester 2-(2-Fluoro-benzenesulfonyl)-octahydro-pyrido[1,2-a]pyrazin-6-one (3S,6R)-3-Benzyl-1,4-diazabicyclo<4.4.0>decane-2,5-dione