摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

3-(2-Chloro-ethyl)-8-methanesulfonyl-3H-pyrazolo[5,1-d][1,2,3,5]tetrazin-4-one | 90521-40-7

中文名称
——
中文别名
——
英文名称
3-(2-Chloro-ethyl)-8-methanesulfonyl-3H-pyrazolo[5,1-d][1,2,3,5]tetrazin-4-one
英文别名
3-(2-Chloroethyl)-8-methylsulfonylpyrazolo[5,1-d][1,2,3,5]tetrazin-4-one
3-(2-Chloro-ethyl)-8-methanesulfonyl-3H-pyrazolo[5,1-d][1,2,3,5]tetrazin-4-one化学式
CAS
90521-40-7
化学式
C7H8ClN5O3S
mdl
——
分子量
277.691
InChiKey
DYFOLIVSADVMQX-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):
    0.5
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    105
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    5-diazo-(4-methylsulfony)pyrazole 、 氯乙基异氰酸酯 反应 24.0h, 以48%的产率得到3-(2-Chloro-ethyl)-8-methanesulfonyl-3H-pyrazolo[5,1-d][1,2,3,5]tetrazin-4-one
    参考文献:
    名称:
    Antitumor imidazotetrazines. 14. Synthesis and antitumor activity of 6- and 8-substituted imidazo[5,1-d]-1,2,3,5-tetrazinones and 8-substituted pyrazolo[5,1-d]-1,2,3,5-tetrazinones
    摘要:
    The systematic variation of the potent antitumor agent mitozolomide (1) is extended to cover alteration of substituents at positions 6 and 8 and to change the imidazo[5,1-d]-1,2,3,5-tetrazinone (1) skeleton to the isomeric pyrazolo-[5,1-d]-1,2,3,5-tetrazinone (17) skeleton. The series of eight 6-alkyl and 6-aralkyl derivatives of 1 showed optimal antitumor activity when the group was small or linear, but activity diminished as size and branching of this substituent increased. This may reflect altered transport characteristics, or failure of the enlarged derivatives to fit a binding site, or possibly a reduced tendency for the derivatives having bulky groups at position 6 to hydrolytically generate the putatively active triazenes (21). Testing of 14 derivatives of 1 differently substituted at position 8 revealed a complex structure-activity relationship, with good antitumor activity obtained for carbamoyl and sulfamoyl groups bearing small substituents. The 8-methylsulfonyl compound had noteworthy activity, but the 8-cyano, 8-nitro, and 8-phenyl derivatives were devoid of useful antitumor activity in these tests. From the limited number of pyrazolotetrazinones (17) reported here, it is suggested that the same conclusions as regards activity also hold true for this ring system.
    DOI:
    10.1021/jm00385a018
点击查看最新优质反应信息

文献信息

  • LUNT E.; NEWTON CH. G.; SMITH CH.; STEVENS G. P.; STEVENS M. F. G.; STRAW+, J. MED. CHEM., 30,(1987) N 2, 357-366
    作者:LUNT E.、 NEWTON CH. G.、 SMITH CH.、 STEVENS G. P.、 STEVENS M. F. G.、 STRAW+
    DOI:——
    日期:——
查看更多

同类化合物

酪氨酸,2-甲氧基-O-甲基- 达美司特 百里酚-6-磺化三(2-羟基乙基)铵 吡唑并[1,5-a][1,3,5]噻嗪-4(3H)-酮 吡唑并[1,5-a][1,3,5]三嗪-2,4-二胺 吡唑并[1,5-a]-1,3,5-三嗪-4-胺,N-羟基- 吡唑并[1,5-D][1,2,4]三嗪酮 吡唑并[1,5-A]-1,3,5-三嗪-2,4(1H,3H)-二酮 N4-(1,1-二甲基乙基)-7-甲基吡唑并(1,5-a)-1,3,5-三嗪-2,4-二胺盐酸盐 N'-甲酰基-4-氨基吡唑并[5,1-c][1,2,4]三嗪-3-甲酰肼 8-苄基-2-甲基-4-(N-甲基氨基)吡唑并[1,5-a]-1,3,5-三嗪 8-碘-1H,4H-吡唑并[1,5-a][1,3,5]三嗪-4-酮 8-溴-4-氯-2-(甲基硫代)吡唑并[1,5-a][1,3,5]三嗪 8-溴-2-(甲基硫代)吡唑并[1,5-a][1,3,5]噻嗪-4-醇 8-溴-2,7-二甲基-3H-吡唑并[1,5-a][1,3,5]噻嗪-4-酮 8-溴-1H,4H-吡唑并[1,5-a][1,3,5]三嗪-4-酮 7-甲基-吡唑并[1,5-a]-1,3,5-三嗪-4(1H)-酮 7-甲基-6H-吡唑并[4,5-e][1,2,3]三嗪-4-酮 7-甲基-1,7-二氢-4H-吡唑并[3,4-d][1,2,3]三嗪-4-酮2-氧化物 7-(叔丁基)吡唑并[1,5-a][1,3,5]三嗪-4(3H)-酮 5-二乙基氨基甲基-2-苯基呋喃-3-羧酸 5,6-二氢吡唑并[1,5-d][1,2,4]三嗪-4,7-二酮 4-甲氧基吡唑并[1,5-a][1,3,5]三嗪 4-氯-2-(甲硫基)吡唑并[1,5-a][1,3,5]三嗪 4-氨基-7-甲基吡唑并[5,1-C][1,2,4]三嗪-3-甲腈 4,7-二甲基吡唑并[5,1-c][1,2,4]三嗪-3-羧酸乙酯 4,7-二甲基吡唑并[5,1-C][1,2,4]三嗪-3-羧酸 4,6-二氢-6-(碘乙酰基)-3-甲基-4-亚甲基吡唑并[5,1-c][1,2,4]三嗪 3-甲氧基-2H-吡唑并[4,3-e][1,2,4]三嗪 3-(1,1-二甲基乙基)-7-(5-甲基-3-异恶唑基)-2-[(1-甲基-1H-1,2,4-三唑-5-基)甲氧基]吡唑并[1,5-d][1,2,4]三嗪 3,4-二甲基吡唑并[5,1-c][1,2,4]三嗪 2-甲基吡唑并[1,5-d][1,2,4]三嗪-4(5H)-酮 2-甲基吡唑并[1,5-a][1,3,5]三嗪-4(1H)-酮 2-甲基-4-(N-甲基氨基)-8-[(2-噻吩基)甲基]吡唑并[1,5-a]-1,3,5-三嗪 2-氨基吡唑并[1,5-a][1,3,5]三嗪-4(1H)-酮 2-Thi氧代-2,3-二氢吡唑并[1,5-a][1,3,5]噻嗪-4(1H)-酮 2-(甲基硫代)吡唑并[1,5-a][1,3,5]噻嗪-4(3H)-酮 2,4-二氨基-吡唑并(1,5-a)-S-三嗪盐酸盐半水合物 2,4-二(甲基氨基)-7-甲基吡唑并(1,5-a)-S-三嗪 1-(4,7-二甲基吡唑并[5,1-c][1,2,4]三氮杂-3-基)-1-乙酮 4-chloro-2-methylpyrazolo[1,5-a][1,3,5]triazine 8,9-Bis-(2-furyl)furo<3,2-d>-s-triazolo<4,3-c>pyrimidin N,N-dimethyl-N'-[7-methyl-3-(5-nitro-furan-2-yl)-[1,2,4]triazolo[4,3-c]pyrimidin-5-yl]-formamidine (8-chloro-7-methyl-pyrazolo[1,5-a][1,3,5]triazin-4-yl)-methyl-amine methyl-phosphonothioic acid O-isopropyl ester O'-{1-[6-oxo-4-(1,1,2,2-tetrafluoro-ethoxy)-phenyl]-1,6-dihydro-pyridazin-3-yl} ester 9-bromo-3-phenyl-pyridazino[1,6-a][1,3,5]triazine-2,4-dione prop-2-ynyl 5-(1H-benzo[d][1,2,3]triazol-5-yl)-7-oxo-4,7-dihydropyrazolo[1,5-a]pyrimidine-3-carbimidate hydrochloride 6-Acetyl-3-methyl-4-methylen-pyrazolo<3,2-c>-as-triazin 2-Methylamino-5,7-dimethyl-s-triazolo<2,3-c>pyrimidin ethyl 7-benzamido-3-tert-butyl-4-oxo-4,6-dihydropyrazolo[5,1-c][1,2,4]triazine-8-carboxylate