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tert-butyl N-[(2S,3R)-1-cyclohexyl-3-hydroxy-4-imidazo[1,5-a]pyridin-3-ylsulfanylbutan-2-yl]carbamate | 141463-19-6

中文名称
——
中文别名
——
英文名称
tert-butyl N-[(2S,3R)-1-cyclohexyl-3-hydroxy-4-imidazo[1,5-a]pyridin-3-ylsulfanylbutan-2-yl]carbamate
英文别名
——
tert-butyl N-[(2S,3R)-1-cyclohexyl-3-hydroxy-4-imidazo[1,5-a]pyridin-3-ylsulfanylbutan-2-yl]carbamate化学式
CAS
141463-19-6
化学式
C22H33N3O3S
mdl
——
分子量
419.588
InChiKey
HLJWMLNJIBTWGF-OALUTQOASA-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):
    4.65
  • 重原子数:
    29.0
  • 可旋转键数:
    7.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    75.86
  • 氢给体数:
    2.0
  • 氢受体数:
    6.0

反应信息

  • 作为反应物:
    描述:
    tert-butyl N-[(2S,3R)-1-cyclohexyl-3-hydroxy-4-imidazo[1,5-a]pyridin-3-ylsulfanylbutan-2-yl]carbamate 、 (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate 、 三乙胺三氟乙酸 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 6.0h, 生成 {1-[1-[1-Cyclohexylmethyl-2-hydroxy-3-(imidazo[1,5-a]pyridin-3-ylsulfanyl)-propylcarbamoyl]-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester; hydrate
    参考文献:
    名称:
    Renin inhibitors containing C-termini derived from mercaptoheterocycles
    摘要:
    A series of transition-state analogues having heterocyclylthio C-termini has been synthesized and evaluated for inhibition of human renin. Addition of mercaptoheterocycles to a chiral Boc-amino epoxide intermediate led, after several steps, to the target [(2R,3S)-3-(BocPheHis-amino)-4-cyclohexyl-2-hydroxy-1-butyl]thio derivatives. Oxidation of the thioether to sulfone was also investigated. Several of the compounds, especially those derived from N1-substituted-5-mercaptotetrazoles or N4-substituted-3-mercapto-5-(trifluoromethyl)-1,2,4-triazoles, were moderately potent inhibitors of human plasma renin, having IC50 values of 30-40 nM. When selected compounds were administered intravenously to sodium-deficient rhesus monkeys at 0.3-1.2 mg/kg, they reduced plasma renin activity by 75-98%. However, this inhibition and the accompanying drop in blood pressure were of short duration.
    DOI:
    10.1021/jm00089a023
  • 作为产物:
    描述:
    咪唑并[1,5-a]吡啶-3(2H)-硫酮(2R,3S)-3-(t-butoxycarbonylamino)-4-cyclohexyl-1,2-epoxybutaneN-甲基吗啉 作用下, 以 乙腈 为溶剂, 反应 2.0h, 以65%的产率得到tert-butyl N-[(2S,3R)-1-cyclohexyl-3-hydroxy-4-imidazo[1,5-a]pyridin-3-ylsulfanylbutan-2-yl]carbamate
    参考文献:
    名称:
    Renin inhibitors containing C-termini derived from mercaptoheterocycles
    摘要:
    A series of transition-state analogues having heterocyclylthio C-termini has been synthesized and evaluated for inhibition of human renin. Addition of mercaptoheterocycles to a chiral Boc-amino epoxide intermediate led, after several steps, to the target [(2R,3S)-3-(BocPheHis-amino)-4-cyclohexyl-2-hydroxy-1-butyl]thio derivatives. Oxidation of the thioether to sulfone was also investigated. Several of the compounds, especially those derived from N1-substituted-5-mercaptotetrazoles or N4-substituted-3-mercapto-5-(trifluoromethyl)-1,2,4-triazoles, were moderately potent inhibitors of human plasma renin, having IC50 values of 30-40 nM. When selected compounds were administered intravenously to sodium-deficient rhesus monkeys at 0.3-1.2 mg/kg, they reduced plasma renin activity by 75-98%. However, this inhibition and the accompanying drop in blood pressure were of short duration.
    DOI:
    10.1021/jm00089a023
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同类化合物

阿法拉定A,TFA 钠咪唑并[1,2-a]吡啶-2-羧酸酯水合物(1:1:1) 钠(E)-2-氰基-3-[2,8-二(丙-2-基氧基)咪唑并[3,2-a]吡啶-3-基]丙-2-烯酸酯 诺白拉斯啶 苯酚,4-(5,6,7,8-四氢咪唑并[1,2-a]吡啶-8-基)- 米诺膦酸 米诺磷酸一水合物 硫酸利美戈潘 盐酸法屈唑半水合物 盐酸依格列汀 甲基咪唑并[1,5-A]吡啶-1-甲酸叔丁酯 甲基3-氨基咪唑并[1,2-a]吡啶-5-羧酸酯 甲基-(7-甲基咪唑并[1,2-A〕吡啶-2-基甲基)-胺 甲基-(5-甲基-咪唑并[1,2-A]吡啶-2-甲基)-胺 甲基 2-甲基咪唑并[1,2-a]吡啶-3-羧酸 环戊烷羧酸2-氨基-4-亚甲基-,(1R,2S)-(9CI) 环巴胺抑制剂1 泰妥拉唑 法倔唑盐酸盐 法倔唑 沃利替尼(对映异构体) 沃利替尼 氨基膦酸杂质14 戊酰胺,N-(2-丁基-1H-咪唑并[4,5-b]吡啶-6-基)- 巴马鲁唑 奥克塞米索 地扎胍宁甲磺酸盐 地扎胍宁 土大黄甙 咪唑磺隆 咪唑并吡啶-6-甲胺盐酸盐 咪唑并吡啶-2-酮盐酸盐 咪唑并吡啶-2-酮 咪唑并二甲基吡啶 咪唑并[2,1-a]异喹啉-2(3H)-酮 咪唑并[1,5-a]喹唑啉,6-氯-3-(3-环丙基-1,2,4-噁二唑-5-基)-5-(4-吗啉基)- 咪唑并[1,5-a]吡啶-8-胺 咪唑并[1,5-a]吡啶-8-羧酸乙酯 咪唑并[1,5-a]吡啶-8-甲醛 咪唑并[1,5-a]吡啶-7-羧酸甲酯 咪唑并[1,5-a]吡啶-7-羧酸乙酯 咪唑并[1,5-a]吡啶-6-羧酸甲酯 咪唑并[1,5-a]吡啶-6-羧酸乙酯 咪唑并[1,5-a]吡啶-5-胺 咪唑并[1,5-a]吡啶-5-羧酸甲酯 咪唑并[1,5-a]吡啶-5-羧酸乙酯 咪唑并[1,5-a]吡啶-5-甲醛 咪唑并[1,5-a]吡啶-3-羧酸乙酯 咪唑并[1,5-a]吡啶-3-磺酰胺 咪唑并[1,5-a]吡啶-3-甲醛