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(+/-)-7-(4-Oxo-2-pyrimidin-4-yl-5,6,8,9-tetrahydro-4H-7-oxa-1,4a-diaza-benzocyclohepten-9-ylcarbamoyl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester | 1175532-16-7

中文名称
——
中文别名
——
英文名称
(+/-)-7-(4-Oxo-2-pyrimidin-4-yl-5,6,8,9-tetrahydro-4H-7-oxa-1,4a-diaza-benzocyclohepten-9-ylcarbamoyl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester
英文别名
(+/-)-7-(4-Oxo-2-pyrimidin-4-yl-5,6,8,9-tetrahydro-4H-7-oxa-1,4-a-diaza-benzocyclohepten-9-ylcarbamoyl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester;tert-butyl 7-[(4-oxo-2-pyrimidin-4-yl-6,7,9,10-tetrahydropyrimido[1,2-d][1,4]oxazepin-10-yl)carbamoyl]-3,4-dihydro-1H-isoquinoline-2-carboxylate
(+/-)-7-(4-Oxo-2-pyrimidin-4-yl-5,6,8,9-tetrahydro-4H-7-oxa-1,4a-diaza-benzocyclohepten-9-ylcarbamoyl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester化学式
CAS
1175532-16-7
化学式
C27H30N6O5
mdl
——
分子量
518.572
InChiKey
OUNQWDLWDRSKGP-UHFFFAOYSA-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):
    0.8
  • 重原子数:
    38
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    126
  • 氢给体数:
    1
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    (+/-)-7-(4-Oxo-2-pyrimidin-4-yl-5,6,8,9-tetrahydro-4H-7-oxa-1,4a-diaza-benzocyclohepten-9-ylcarbamoyl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester盐酸 作用下, 以 1,4-二氧六环二氯甲烷 为溶剂, 反应 2.5h, 以70%的产率得到1,2,3,4-Tetrahydro-isoquinoline-7-carboxylic acid (4-oxo-2-pyrimidin-4-yl-5,6,8,9-tetrahydro-4H-7-oxa-1,4a-diaza-benzocyclohepten-9-yl)-amide hydrochloride
    参考文献:
    名称:
    Substituted heteroarylamide oxazepinopyrimidone derivatives
    摘要:
    一种由式(I)表示的吡啶酮衍生物或其盐,或其溶剂或水合物: 其中: Y代表两个氢原子,一个硫原子,一个氧原子或一个C1-2烷基和一个氢原子; Z代表键,一个氧原子,一个氮原子,该氮原子被一个氢原子或C1-3烷基取代,一个硫原子,一个亚甲基,该亚甲基可选地被选自C1-6烷基,羟基,C1-6烷氧基,C1-2全氟烷基或氨基的一或两个基团取代; R1代表2、3或4-吡啶环或2、4或5-嘧啶环,该环可选地被C1-6烷基,C1-6烷氧基或卤素原子取代; R2代表氢原子,C1-6烷基或卤素原子; R3代表4-15成员的杂环基,该基团可选地被取代; R4代表氢原子或C1-6烷基; n代表0到3及其治疗用途。
    公开号:
    EP2085400A1
  • 作为产物:
    描述:
    2-BOC-7-羧基-1,2,3,4-四氢异喹啉 、 (+/-)-9-amino-2-pyrimidin-4-yl-5,6,8,9-tetrahydro-7-oxa-1,4a-diaza-benzocyclohepten-4-one 在 氰基磷酸二乙酯三乙胺 作用下, 以 乙酸乙酯N,N-二甲基甲酰胺 为溶剂, 反应 15.0h, 以38%的产率得到(+/-)-7-(4-Oxo-2-pyrimidin-4-yl-5,6,8,9-tetrahydro-4H-7-oxa-1,4a-diaza-benzocyclohepten-9-ylcarbamoyl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester
    参考文献:
    名称:
    Substituted heteroarylamide oxazepinopyrimidone derivatives
    摘要:
    一种由式(I)表示的吡啶酮衍生物或其盐,或其溶剂或水合物: 其中: Y代表两个氢原子,一个硫原子,一个氧原子或一个C1-2烷基和一个氢原子; Z代表键,一个氧原子,一个氮原子,该氮原子被一个氢原子或C1-3烷基取代,一个硫原子,一个亚甲基,该亚甲基可选地被选自C1-6烷基,羟基,C1-6烷氧基,C1-2全氟烷基或氨基的一或两个基团取代; R1代表2、3或4-吡啶环或2、4或5-嘧啶环,该环可选地被C1-6烷基,C1-6烷氧基或卤素原子取代; R2代表氢原子,C1-6烷基或卤素原子; R3代表4-15成员的杂环基,该基团可选地被取代; R4代表氢原子或C1-6烷基; n代表0到3及其治疗用途。
    公开号:
    EP2085400A1
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文献信息

  • SUBSTITUTED HETEROARYLAMIDE OXAZEPINOPYRIMIDONE DERIVATIVES
    申请人:FAYOL Aude
    公开号:US20110015176A1
    公开(公告)日:2011-01-20
    The disclosure relates to a series pyrimidone derivatives represented by formula (I) or a salt thereof, or a solvate thereof or a hydrate thereof: wherein: Y, Z, R1, R2, R3, R4 and n are as defined in the disclosure. Also disclosed are methods of preparing the compounds of formula (I), intermediates therefor and their utility in treating a variety of disease conditions.
    本公开涉及一系列以式(I)表示的嘧啶酮衍生物或其盐、溶剂或水合物:其中:Y、Z、R1、R2、R3、R4和n如本公开所定义。同时还公开了制备式(I)化合物的方法、其中间体以及它们在治疗各种疾病状况中的用途。
  • US8501728B2
    申请人:——
    公开号:US8501728B2
    公开(公告)日:2013-08-06
  • [EN] SUBSTITUTED HETEROARYLAMIDE OXAZEPINOPYRIMIDONE DERIVATIVES<br/>[FR] DÉRIVÉS D'HÉTÉROARYLAMIDE OXAZÉPINOPYRIMIDONE SUBSTITUÉS
    申请人:SANOFI AVENTIS
    公开号:WO2009095787A1
    公开(公告)日:2009-08-06
    A pyrimidone derivative represented by Formula (I) or a salt thereof, or a solvate thereof or a hydrate thereof: Formula (I) wherein: Y represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C1-2 alkyl group and a hydrogen atom; Z represents a bond, an oxygen atom, a nitrogen atom substituted by a hydrogen atom or a C1-3 alkyl group, a sulphur atom, a methylene group optionally substituted by one or two groups chosen from a Ci-6 alkyl group, a hydroxyl group, a C1-6 alkoxy group, a C1-2 perhalogenated alkyl group or an amino group; R1 represents a 2, 3 or 4-pyridine ring or a 2, 4 or 5-pyrimidine ring, the ring being optionally substituted by a C1-6 alkyl group, a C1-6 alkoxy group or a halogen atom; R2 represents a hydrogen atom, a C1-6 alkyl group or a halogen atom; R3 represents a 4-15 membered heterocyclic group, this group being optionally substituted; R4 represents a hydrogen atom or a C1-6 alkyl group; and n represents 0 to 3 and their therapeutic use.
  • Substituted heteroarylamide oxazepinopyrimidone derivatives
    申请人:Sanofi-Aventis
    公开号:EP2085400A1
    公开(公告)日:2009-08-05
    A pyrimidone derivative represented by formula (I) or a salt thereof, or a solvate thereof or a hydrate thereof: wherein: Y represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C1-2 alkyl group and a hydrogen atom; Z represents a bond, an oxygen atom, a nitrogen atom substituted by a hydrogen atom or a C1-3 alkyl group, a sulphur atom, a methylene group optionally substituted by one or two groups chosen from a C1-6 alkyl group, a hydroxyl group, a C1-6 alkoxy group, a C1-2 perhalogenated alkyl group or an amino group; R1 represents a 2, 3 or 4-pyridine ring or a 2, 4 or 5-pyrimidine ring, the ring being optionally substituted by a C1-6 alkyl group, a C1-6 alkoxy group or a halogen atom; R2 represents a hydrogen atom, a C1-6 alkyl group or a halogen atom; R3 represents a 4-15 membered heterocyclic group, this group being optionally substituted; R4 represents a hydrogen atom or a C1-6 alkyl group; and n represents 0 to 3 and their therapeutic use.
    一种由式(I)表示的吡啶酮衍生物或其盐,或其溶剂或水合物: 其中: Y代表两个氢原子,一个硫原子,一个氧原子或一个C1-2烷基和一个氢原子; Z代表键,一个氧原子,一个氮原子,该氮原子被一个氢原子或C1-3烷基取代,一个硫原子,一个亚甲基,该亚甲基可选地被选自C1-6烷基,羟基,C1-6烷氧基,C1-2全氟烷基或氨基的一或两个基团取代; R1代表2、3或4-吡啶环或2、4或5-嘧啶环,该环可选地被C1-6烷基,C1-6烷氧基或卤素原子取代; R2代表氢原子,C1-6烷基或卤素原子; R3代表4-15成员的杂环基,该基团可选地被取代; R4代表氢原子或C1-6烷基; n代表0到3及其治疗用途。
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