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2-[(E)-tert-Butoxycarbonylimino]-5-cyano-4-methyl-2H-pyrimidine-1-carboxylic acid tert-butyl ester | 454483-77-3

中文名称
——
中文别名
——
英文名称
2-[(E)-tert-Butoxycarbonylimino]-5-cyano-4-methyl-2H-pyrimidine-1-carboxylic acid tert-butyl ester
英文别名
——
2-[(E)-tert-Butoxycarbonylimino]-5-cyano-4-methyl-2H-pyrimidine-1-carboxylic acid tert-butyl ester化学式
CAS
454483-77-3
化学式
C16H22N4O4
mdl
——
分子量
334.375
InChiKey
OOROORAMCSNZRS-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):
    2.68
  • 重原子数:
    24.0
  • 可旋转键数:
    0.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    106.57
  • 氢给体数:
    0.0
  • 氢受体数:
    7.0

反应信息

  • 作为反应物:
    描述:
    2-[(E)-tert-Butoxycarbonylimino]-5-cyano-4-methyl-2H-pyrimidine-1-carboxylic acid tert-butyl ester 在 palladium on activated charcoal 盐酸氢气 作用下, 以 乙醇 为溶剂, 反应 16.0h, 生成
    参考文献:
    名称:
    Non-covalent thrombin inhibitors featuring p 3 -heterocycles with P 1 -monocyclic arginine surrogates
    摘要:
    Investigations on P-2-P-3-heterocyclic dipeptide surrogates directed towards identification of an orally bioavailable thrombin inhibitor led us to pursue novel classes of achiral, non-covalent P-1-arginine derivatives. The design. synthesis. and biological activity of inhibitors NC1-NC30 that feature three classes of monocyclic P-1-arginine surrogates will be disclosed: (1) (hetero)aromatic amidines, amines and hydrox amidines, (2) 2-aminopyrazines. and (3) 2-aminopyrimidines and 2-aminotetrahydropyrimidines. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(02)00129-4
  • 作为产物:
    参考文献:
    名称:
    Non-covalent thrombin inhibitors featuring p 3 -heterocycles with P 1 -monocyclic arginine surrogates
    摘要:
    Investigations on P-2-P-3-heterocyclic dipeptide surrogates directed towards identification of an orally bioavailable thrombin inhibitor led us to pursue novel classes of achiral, non-covalent P-1-arginine derivatives. The design. synthesis. and biological activity of inhibitors NC1-NC30 that feature three classes of monocyclic P-1-arginine surrogates will be disclosed: (1) (hetero)aromatic amidines, amines and hydrox amidines, (2) 2-aminopyrazines. and (3) 2-aminopyrimidines and 2-aminotetrahydropyrimidines. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(02)00129-4
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