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tert-butyl 2-amino-4H-pyrrolo[3,2-d]thiazole-4-carboxylate | 1209492-79-4

中文名称
——
中文别名
——
英文名称
tert-butyl 2-amino-4H-pyrrolo[3,2-d]thiazole-4-carboxylate
英文别名
4-Boc-4H-pyrrolo[3,2-d]thiazol-2-amine;tert-butyl 2-aminopyrrolo[3,2-d][1,3]thiazole-4-carboxylate
tert-butyl 2-amino-4H-pyrrolo[3,2-d]thiazole-4-carboxylate化学式
CAS
1209492-79-4
化学式
C10H13N3O2S
mdl
——
分子量
239.298
InChiKey
CNXQPCLPWQBQJX-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):
    2.4
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    98.4
  • 氢给体数:
    1
  • 氢受体数:
    5

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • 并环含氮化合物、其中间体、制备方法和应用
    申请人:杭州圣域生物医药科技有限公司
    公开号:CN117946138A
    公开(公告)日:2024-04-30
    本发明公开了一种并环含氮化合物、其中间体、制备方法和应用。本发明提供了一种如式I所示的化合物、其药学上可接受的盐或同位素化合物。本发明的化合物的ATPase活性和对蛋白的抑制效果较现有技术有较大改善。#imgabs0#
  • RING-FUSED AZOLE DERIVATIVE HAVING PI3K-INHIBITING ACTIVITY
    申请人:Mitsuoka Yasunori
    公开号:US20110230472A1
    公开(公告)日:2011-09-22
    It is an object of the present invention to provide a compound or a pharmaceutically acceptable salt thereof which inhibits the activity of PI3K to regulate many biological processes including the growth, differentiation, survival, proliferation, migration, metabolism, and the like of cells and is therefore useful for the prophylaxis/therapy of diseases including inflammatory diseases, arteriosclerosis, vascular/circulatory diseases, cancer/tumors, immune system diseases, cell proliferative diseases, infectious diseases, and the like. The above problem was solved by providing a ring-fused azole compound shown in the present specification, or a pharmaceutically acceptable salt thereof.
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同类化合物

4H-吡咯并[2.3-d][1,3]噻唑-5-羧酸乙酯 4H-吡咯并[2,3-d]噻唑-5-羧酸 4H-吡咯并[2,3-d]噻唑 (7aS)-1-(1-cyanoethenyl)tetrahydro-1H,3H-pyrrolo[1,2-c]thiazole-3-thione 4-methyl-4,6-dihydro-5H-thiazolo[5‘,4‘:4,5]pyrrolo[2,3-d]pyridazin-5-one 3-((2,4-dimethyl-5-oxo-4H-thiazolo[5’,4’:4,5]pyrrolo[2,3-d]pyridazin-6(5H)-yl)methyl)benzonitrile 7-propyl-7H-3,4-dithia-1,6,7-triazacyclopenta[a]pentalene 7-propyl-2,5-bis(trimethylstannyl)-7H-3,4-dithia-1,6,7-triazacyclopenta[a]pentalene 4-methyl-4H-pyrrolo[2,3-d]thiazole-5-carboxylic acid 3-morpholino-4-(2,4,5-trimethyl-4H-pyrrolo[3,2-d][1,3]thiazol-6-yl)cyclobut-3-ene-1,2-dione (S)-3-thia-1-azabicyclo[3.3.0]octan-2-one 3,3-dioxide methyl 4H-pyrrolo[2,3-d]thiazole-5-carboxylate (4H-pyrrolo[2,3-d]thiazol-5-yl)methanol 5-methyl-4H-pyrrolo[2,3-d]thiazole tert-butyl 2-amino-4H-pyrrolo[3,2-d]thiazole-4-carboxylate 2-ethoxycarbonylamino-4-methyl-4H-pyrrolo[3,2-d]thiazole-5-carboxylic acid methyl ester (4-methyl-6-nitro-4H-pyrrolo[2,3-d]thiazol-2-yl)-carbamic acid ethyl ester 2-ethoxycarbonylamino-4-methyl-4H-pyrrolo[3,2-d]thiazole-5-carboxylic acid ethyl ester (5-bromo-4-methyl-6-nitro-4H-pyrrolo[3,2-d]thiazol-2-yl)-carbamic acid ethyl ester 2-Ethoxycarbonylamino-4-methylpyrrolo<3,2-d>thiazol (Z)-2-[(methylsulfonyl)methylidene]pyrrolidino[2,1-c]thiazolidine (5-bromo-4-methyl-6-nitro-4H-pyrrolo[2,3-d]thiazol-2-yl)-carbamic acid ethyl ester ethyl 2-methyl-4H-pyrrolo[3,2-d]thiazole-5-carboxylate ethyl 5-methyl-5H-pyrrolo[3,4-d]thiazolo-2-carboxylate 2-phenyl-4H-pyrrolo[3,2-d]thiazole-5-carboxylic acid ethyl ester 5-benzyl-4H-pyrrolo[2,3-d]thiazole 4-(4H-pyrrolo[2,3-d]thiazol-5-yl)pyridin-2-ylamine ethyl 4H-pyrrolo[3,2-d]thiazole-5-carboxylate 2,6-dibromo-4-(2-octyldodecyl)-4H-pyrrolo[3,2-d:4,5-d]bisthiazole tetrahydro-pyrrolo[1,2-c]thiazole-3-thione (-)-(1R,7aS)-1-methyltetrahydropyrrolo[1,2-c]thiazol-3(1H)-thione (-)-(1S,7aS)-1-methyltetrahydropyrrolo[1,2-c]thiazol-3(1H)-thione methyl (2R,6R,7R,8S,11R)-5-oxo-11-phenyl-10-thia-1-azatricyclo[6.3.0.02,6]undecane-7-carboxylate (2R,6R,7R,8S,11R)-11-phenyl-7-[(E)-2-phenylethenyl]-10-thia-1-azatricyclo[6.3.0.02,6]undecan-5-one N-[[4-(propan-2-ylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide N-[[4-(pyridin-2-ylmethylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide N-[[4-(morpholine-4-carbonyl)cyclohexyl]methyl]-4H-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide N-[[4-(thiophen-2-ylmethylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide N-[[4-(pyridin-2-ylmethylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide N-[[4-(morpholine-4-carbonyl)cyclohexyl]methyl]-4H-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide N-[[4-(cyclopropylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide N-[[4-(furan-2-ylmethylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide N-[[4-(pyrrolidine-1-carbonyl)cyclohexyl]methyl]-4H-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide (1S,2S,7S,8R)-10-[2-[[3-chloro-5-(trifluoromethyl)pyridin-2-yl]amino]ethyl]-7-[(E)-2-phenylethenyl]-4-thia-6,10-diazatricyclo[6.3.0.02,6]undecane-9,11-dione (1S,2S,7R,8R)-10-[2-[[3-chloro-5-(trifluoromethyl)pyridin-2-yl]amino]ethyl]-7-[(E)-2-phenylethenyl]-4-thia-6,10-diazatricyclo[6.3.0.02,6]undecane-9,11-dione 4-[(3,4-Dichlorophenyl)methyl]pyrrolo[2,3-d][1,3]thiazole-5-carboxylic acid 2-(4H-pyrrolo[2,3-d][1,3]thiazol-5-yl)acetic acid Methyl 4-(3,4-dichlorobenzyl)-2-methyl-4 H-pyrrolo[3,2-d ][1,3]thiazole-5-carboxylate Ethyl 4-[(3,4-dichlorophenyl)methyl]pyrrolo[2,3-d][1,3]thiazole-5-carboxylate methyl 4-(3,4-dichlorobenzyl)-4H-pyrrolo[3,2-d][1,3]thiazole-5-carboxylate