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2,6-Diamino-4-phenyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-ethyl ester 5-isopropyl ester | 50698-40-3

中文名称
——
中文别名
——
英文名称
2,6-Diamino-4-phenyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-ethyl ester 5-isopropyl ester
英文别名
2,6-Diamino-4-phenyl-1,4-dihydropyridine-3,5-dicarboxylic acid 3-ethyl ester 5-isopropyl ester;3-O-ethyl 5-O-propan-2-yl 2,6-diamino-4-phenyl-1,4-dihydropyridine-3,5-dicarboxylate
2,6-Diamino-4-phenyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-ethyl ester 5-isopropyl ester化学式
CAS
50698-40-3
化学式
C18H23N3O4
mdl
——
分子量
345.398
InChiKey
YTOUMFPDHOONDU-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):
    3.1
  • 重原子数:
    25
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    117
  • 氢给体数:
    3
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    α-氰基肉桂酸乙酯 、 amidinoacetic acid isopropyl ester 、 sodium ethanolate乙醇 为溶剂, 反应 4.0h, 以2,6-diamino-4-phenyl-1,4-dihydropyridine-3,5-dicarboxylic acid 3-ethyl ester 5-isopropyl ester of m.p. 170° is obtained的产率得到2,6-Diamino-4-phenyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-ethyl ester 5-isopropyl ester
    参考文献:
    名称:
    2,6-Diamino-1,4-dihydropyridine derivatives
    摘要:
    具有3-和5-位上的羰基功能,并在4-位上被低碳基,苯基,取代苯基或杂环基替代的2,6-二氨基-1,4-二氢吡啶是抗高血压药物和冠状血管扩张剂。这些化合物,其中2,6-二氨基-4-(3-硝基苯基)-1,4-二氢吡啶-3,5-二羧酸3,5-二乙酯是代表性实施例,是通过将脒与醛或乙烯基氰乙酮酸酯缩合而制备的。
    公开号:
    US03950336A1
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文献信息

  • Use of 2,6-diamino-4-substituted-1,4-dihydropyridine-3,5-dicarboxylic
    申请人:Bayer Aktiengesellschaft
    公开号:US03957998A1
    公开(公告)日:1976-05-18
    2,6-Diamino-1,4-dihydropyridines bearing carbonyl functions in the 3- and 5-positions and being substituted in the 4-position by lower alkyl, phenyl, substituted phenyl or a heterocyclic group are antihypertensive agents and coronary vessel dilators. The compounds, of which 2,6-diamino-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid 3,5-diethyl ester is a representative embodiment, are prepared through condensation of an amidine with either an aldehyde or an ylidenecyanoacetoacetic acid ester.
    2,6-二基-1,4-二氢吡啶在3和5位带有羰基功能,且在4位被低级烷基,苯基,取代苯基或杂环基取代,是降压剂和冠状血管扩张剂。这些化合物,其中2,6-二基-4-(3-硝基苯基)-1,4-二氢吡啶-3,5-二羧酸3,5-二乙酯是代表性的实施例,是通过将一种与醛或伊利丹乙酰乙酸酯缩合制备而成。
  • 2,6-Diamino-1,4-dihydropyridine-3,5-dicarboxylic acid esters used as
    申请人:Bayer Aktiengesellschaft
    公开号:US03959474A1
    公开(公告)日:1976-05-25
    2,6-Diamino-1,4-dihydropyridines bearing carbonyl functions in the 3- and 5-positions and being substituted in the 4-position by lower alkyl, phenyl, substituted phenyl or a heterocyclic group are antihypertensive agents and coronary vessel dilators. The compounds, of which 2,6-diamino-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid 3,5-diethyl ester is a representative embodiment, are prepared through condensation of an amidine with either an aldehyde or an ylidenecyanoacetoacetic acid ester.
    在3和5位带有羰基功能并在4位被低碳链、苯基、取代苯基或杂环基取代的2,6-二基-1,4-二氢吡啶类化合物是抗高血压药物和冠状血管扩张剂。这些化合物通过将氨基嘧啶与醛或亚甲基丙烯腈乙酸酯缩合制备而成,其中2,6-二基-4-(3-硝基苯基)-1,4-二氢吡啶-3,5-二羧酸3,5-二乙酯是代表性的实施例。
  • Bicyclic derivatives of 1,4-dihydropyridine 3,5-carboxylic acid esters
    申请人:Bayer Aktiengesellschaft
    公开号:US03988458A1
    公开(公告)日:1976-10-26
    2,6-Diamino-1,4-dihydropyridines bearing carbonyl functions in the 3- and 5-positions and being substituted in the 4-position by lower alkyl, phenyl, substituted phenyl or a heterocyclic group are antihypertensive agents and coronary vessel dilators. The compounds, of which 2,6-diamino-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid 3,5-diethyl ester is a representative embodiment, are prepared through condensation of an amidine with either an aldehyde or an ylidenecyanoacetoacetic acid ester.
    在3-和5-位置带有羰基功能,并在4-位置被低烷基,苯基,取代苯基或杂环基所取代的2,6-二基-1,4-二氢吡啶是抗高血压药物和冠状血管扩张剂。这些化合物,其中2,6-二基-4-(3-硝基苯基)-1,4-二氢吡啶-3,5-二羧酸3,5-二乙酯是代表性实施例,通过将与醛或腈叶酰乙酸酯缩合而制备。
  • 4-Quinoline and 4-isoquinoline derivatives of
    申请人:Bayer Aktiengesellschaft
    公开号:US04016277A1
    公开(公告)日:1977-04-05
    2,6-Diamino-1,4-dihydropyridines bearing carbonyl functions in the 3- and 5-positions and being substituted in the 4-position by lower alkyl, phenyl, substituted phenyl or a heterocyclic group are antihypertensive agents and coronary vessel dilators. The compounds, of which 2,6-diamino-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid 3,5-diethyl ester is a representative embodiment, are prepared through condensation of an amidine with either an aldehyde or an ylidenecyanoacetoacetic acid ester.
    具有羰基功能的2,6-二基-1,4-二氢吡啶,其3和5位被取代,4位被较低的烷基,苯基,取代的苯基或杂环基所取代,是抗高血压剂和冠状血管扩张剂。这些化合物,其中2,6-二基-4-(3-硝基苯基)-1,4-二氢吡啶-3,5-二羧酸3,5-二乙酯是代表性实施例,是通过将与醛或乙烯基酮酸酯缩合而制备的。
  • 4-Quinoline and isoquinoline substituted 2,6-diamino-1,4-dihydropyridine
    申请人:Bayer Aktiengesellschaft
    公开号:US04049662A1
    公开(公告)日:1977-09-20
    2,6-Diamino-1,4-dihydropyridines bearing carbonyl functions in the 3- and 5-positions and being substituted in the 4-position by lower alkyl, phenyl, substituted phenyl or a heterocyclic group are antihypertensive agents and coronary vessel dilators. The compounds, of which 2,6-diamino-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid 3,5-diethyl ester is a representative embodiment, are prepared through condensation of an amidine with either an aldehyde or an ylidenecyanoacetoacetic acid ester.
    3-和5-位带有羰基功能的2,6-二基-1,4-二氢吡啶,并在4-位被低烷基、苯基、取代苯基或杂环基取代,是降压剂和冠状血管扩张剂。这些化合物,其中2,6-二基-4-(3-硝基苯基)-1,4-二氢吡啶-3,5-二羧酸3,5-二乙酯是一个代表性的实施例,是通过将酰胺与醛或腈基乙酮酸酯缩合制备而成。
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