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-t-butyl-1-thia-3-azacyclohexane | 60035-87-2

中文名称
——
中文别名
——
英文名称
3-t-butyl-1-thia-3-azacyclohexane
英文别名
3-tert.-Butyltetrahydro-1,3-thiazin;3-tert-butyl-[1,3]thiazinane;3-tert-butyl-1-thia-3-aza-cyclohexane;3-Tert-butyl-1,3-thiazinane
3-t-butyl-1-thia-3-azacyclohexane化学式
CAS
60035-87-2
化学式
C8H17NS
mdl
——
分子量
159.296
InChiKey
KXUUXLDJRJIVKX-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):
    2.1
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    28.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    N-(3-bromopropyl)-2-methylpropan-2-amine;hydrobromide 以 为溶剂, 生成 3-t-butyl-1-thia-3-azacyclohexane
    参考文献:
    名称:
    Angiolini,L. et al., Gazzetta Chimica Italiana, 1976, vol. 106, p. 111 - 118
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • Compositions and methods for treating diseases and conditions
    申请人:University of Pittsburgh—Of the Commonwealth System of Higher Education
    公开号:US10487076B2
    公开(公告)日:2019-11-26
    A compound of Formula II, or a salt, ester, solvate, hydrate or prodrug thereof: where: X1 is a branched or unbranched C1-10 alkyl, (CH2)s—NH—(CH2)t, (CH2)s—O—(CH2)t, or (CH2)s—C(NH2)—(CH2)v—NH—(CH2)t, where s, t and v are each, independently an integer from 1 to 5; A and B are each, independently, C6-10aryl, C6-10aryl-C1-6alkyl, C3-9 heteroaryl, or C3-9heteroaryl-C1-6alkyl, each optionally substituted with 1, 2 or 3 independently selected Rg groups; C and D are each, independently, C3-7 cycloalkyl, C3-7 cycloalkyl-C1-6alkyl, C3-7 heterocycloalkyl, C3-7 heterocycloalkyl-C1-6 alkyl, C6-10aryl, C6-10aryl-C1-6alkyl, C3-9 heteroaryl, or C3-9heteroaryl-C1-6alkyl, each optionally substituted with 1, 2 or 3 independently selected Rg groups; each Rg is, independently, halogen, C1-6 alkyl, C1-6 haloalkyl, hydroxyl, C1-6 alkoxy, C1-6 haloalkoxy, amino, C1-6 alkylamino, or di-C1-6alkylamino; and n1 and p1 are each, independently, integers from 1 to 10.
    式 II 的化合物或其盐、酯、溶液、水合物或原药: 其中 X1 是支链或未支链的 C1-10 烷基、(CH2)s-NH-(CH2)t、(CH2)s-O-(CH2)t 或 (CH2)s-C(NH2)-(CH2)v-NH-(CH2)t ,其中 s、t 和 v 各自独立地为 1 至 5 的整数; A 和 B 各自独立为 C6-10 芳基、C6-10 芳基-C1-6烷基、C3-9 杂芳基或 C3-9 杂芳基-C1-6烷基,各自任选被 1、2 或 3 个独立选择的 Rg 基团取代; C 和 D 各自独立为 C3-7 环烷基、C3-7 环烷基-C1-6烷基、C3-7 杂环烷基、C3-7 杂环烷基-C1-6烷基、C6-10 芳基、C6-10 芳基-C1-6烷基、C3-9 杂芳基或 C3-9 异芳基-C1-6烷基,各自任选被 1、2 或 3 个独立选择的 Rg 基团取代; 每个 Rg 独立地是卤素、C1-6 烷基、C1-6 卤代烷基、羟基、C1-6 烷氧基、C1-6 卤代烷氧基、氨基、C1-6 烷基氨基或二-C1-6 烷基氨基;以及 n1 和 p1 各自独立地为 1 至 10 的整数。
  • Thienopyrimidine derivative and use thereof in medicine
    申请人:SUNSHINE LAKE PHARMA CO., LTD.
    公开号:US10759812B2
    公开(公告)日:2020-09-01
    The present invention relates to a thienopyrimidine derivative and use thereof in medicine, and also to a pharmaceutical composition containing the compound. The compound or pharmaceutical composition is used for inhibiting acetyl-CoA carboxylase (ACC). The present invention also relates to a method of preparing such compound and pharmaceutical composition, as well as their use in the treatment or prevention of diseases regulated by acetyl-CoA carboxylase in mammals, especially in humans.
    本发明涉及一种噻吩嘧啶衍生物及其在医学中的用途,还涉及一种含有该化合物的药物组合物。该化合物或药物组合物用于抑制乙酰-CoA 羧化酶(ACC)。本发明还涉及制备这种化合物和药物组合物的方法,以及它们在治疗或预防哺乳动物,特别是人类受乙酰-CoA 羧化酶调节的疾病中的用途。
  • COMPOSITIONS AND METHODS FOR TREATING DISEASES AND CONDITIONS
    申请人:University of Pittsburgh - Of the Commonwealth System of Higher Education
    公开号:US20180134693A1
    公开(公告)日:2018-05-17
    A compound of Formula II, or a salt, ester, solvate, hydrate or prodrug thereof: where: X 1 is a branched or unbranched C 1-10 alkyl, (CH 2 ) s —NH—(CH 2 ) t , (CH 2 ) s —O—(CH 2 ) t , or (CH 2 ) s —C(NH 2 )—(CH 2 ) v —NH—(CH 2 ) t , where s, t and v are each, independently an integer from 1 to 5; A and B are each, independently, C 6-10 aryl, C 6-10 aryl-C 1-6 alkyl, C 3-9 heteroaryl, or C 3-9 heteroaryl-C 1-6 alkyl, each optionally substituted with 1, 2 or 3 independently selected R g groups; C and D are each, independently, C 3-7 cycloalkyl, C 3-7 cycloalkyl-C 1-6 alkyl, C 3-7 heterocycloalkyl, C 3-7 heterocycloalkyl-C 1-6 alkyl, C 6-10 aryl, C 6-10 aryl-C 1-6 alkyl, C 3-9 heteroaryl, or C 3-9 heteroaryl-C 1-6 alkyl, each optionally substituted with 1, 2 or 3 independently selected R g groups; each R g is, independently, halogen, C 1-6 alkyl, C 1-6 haloalkyl, hydroxyl, C 1-6 alkoxy, C 1-6 haloalkoxy, amino, C 1-6 alkylamino, or di-C 1-6 alkylamino; and n 1 and p 1 are each, independently, integers from 1 to 10.
  • THIENOPYRIMIDINE DERIVATIVE AND USE THEREOF IN MEDICINE
    申请人:SUNSHINE LAKE PHARMA CO., LTD.
    公开号:US20190352311A1
    公开(公告)日:2019-11-21
    The present invention relates to a thienopyrimidine derivative and use thereof in medicine, and also to a pharmaceutical composition containing the compound. The compound or pharmaceutical composition is used for inhibiting acetyl-CoA carboxylase (ACC). The present invention also relates to a method of preparing such compound and pharmaceutical composition, as well as their use in the treatment or prevention of diseases regulated by acetyl-CoA carboxylase in mammals, especially in humans.
  • Angiolini,L. et al., Gazzetta Chimica Italiana, 1976, vol. 106, p. 111 - 118
    作者:Angiolini,L. et al.
    DOI:——
    日期:——
查看更多

同类化合物

苯西酮 苯甲酸,4-(4-硫代吗啉基)- 硫代吗啉酮 硫代吗啉盐酸盐 硫代吗啉-4-醇1,1-二氧化物 硫代吗啉-4-甲酰氯-1,1-二氧化物 硫代吗啉-3-基甲醇 硫代吗啉-1-鎓-1-醇 硫代吗啉-1,1-二氧化物 硫代吗啉,4-[4-[[2-(2,4-二氯苯基)-2-(1H-咪唑-1-基甲基)-1,3-二噁戊环-4-基]甲氧基]苯基]-,1-氧化,顺-(9CI) 硫代吗啉,3-乙基-2-甲基- 硫代吗啉 1,1-二氧化物盐酸盐 硫代吗啉 甲基2-乙氧基-6H-1,3-噻嗪-5-羧酸酯 甲基2-(甲基氨基)-4-氧代-5,6-二氢-4H-1,3-噻嗪-6-羧酸酯 甲基(2Z)-3-苄基-2-(苄基亚氨基)-4-氧代-1,3-噻嗪烷-6-羧酸酯 甲基(2Z)-3-异丙基-2-(异丙基亚胺)-4-氧代-1,3-噻嗪烷-6-羧酸酯 巯基吗啉-4-甲酸叔丁酯 四氢-3-甲基-2-苯基-4H-1,3-噻嗪-4-酮1,1-二氧化物 四氢-1,4-噻嗪-3,5-二酮 二苯甲基{5-[(4,6-二脱氧六吡喃糖基)氧代]-2,4,6-三羟基环己烷-1,3-二基}二(甲基氨基甲酸酯) N-甲基四氢-1,2-噻嗪S,S-二氧化物 N-甲基-4-硫代吗啉甲酰胺 N-环己基-5,6-二氢-4H-1,3-噻嗪-2-胺 N-亚硝基硫代吗啉 N-丁基-5,6-二氢-4H-1,3-噻嗪-2-胺 N-Boc-1,4-噻嗪S,S-二氧化物 N-(3-氨基丙基)-硫代吗啉 N-(2-羟基丙基)硫代吗啉 N-(2-羟乙基)吗啉 AMT盐酸盐 6-苄基-2-甲基噻嗪1,1-二氧化物 6-羟基-5,6-二甲基-1,3-噻吖己环-2-硫酮 6-甲基-4-苯基硫代吗啉-3-酮 6-甲基-2-苯基-5,6-二氢-4H-1,3-噻嗪 6-甲基-1,3-噻嗪-2-硫酮 6-异丙基-3-硫代吗啉酮 6-丙基-硫代吗啉-3-酮 6-(丁氧基甲基)-4-苯基硫代吗啉-3-酮 6,6-二甲基-1,4-噻嗪-2,5-二甲酸 5H-[1,3]噻唑并[5,4-h][1,4]苯并噻嗪 5-甲基-6-(吡啶-3-基)硫代吗啉-3-酮盐酸(1:1) 5-溴-1,3-噻嗪-2-硫酮 5-乙基-6-苯基-1,3-噻嗪烷-2,4-二酮 5,6-二氢-[1,3]噻唑并[2,3-c][1,4]噻嗪-8-羧酸乙酯 5,6-二氢-6-甲基-4H-1,3-噻嗪-2-胺 5,6-二氢-4H-1,4-噻嗪-2-羧酸乙酯 5,6-二氢-4H-1,3-噻嗪-2-羧酸甲酯 5,6-二氢-4H-1,3-噻嗪-2-基胺氢溴酸盐 5,6-二氢-4,4-二甲基-2-苯基-4H-1,3-噻嗪