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(7-氯噻唑并[5,4-d]嘧啶-2-基)-(2,6-二甲基苯基)胺 | 871266-79-4

中文名称
(7-氯噻唑并[5,4-d]嘧啶-2-基)-(2,6-二甲基苯基)胺
中文别名
——
英文名称
(7-chloro[1,3]thiazolo[5,4-d]pyrimidin-2-yl)(2,6-dimethylphenyl)amine
英文别名
(7-chloro-thiazolo[5,4-d]pyrimidin-2-yl)-(2,6-dimethyl-phenyl)-amine;(7-Chlorothiazolo[5,4-d]pyrimidin-2-yl)-(2,6-dimethylphenyl)amine;7-chloro-N-(2,6-dimethylphenyl)-[1,3]thiazolo[5,4-d]pyrimidin-2-amine
(7-氯噻唑并[5,4-d]嘧啶-2-基)-(2,6-二甲基苯基)胺化学式
CAS
871266-79-4
化学式
C13H11ClN4S
mdl
——
分子量
290.776
InChiKey
DRBASNCUFMSJAA-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

物化性质

  • 沸点:
    430.8±55.0 °C(Predicted)
  • 密度:
    1.430±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.6
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    78.9
  • 氢给体数:
    1
  • 氢受体数:
    5

SDS

SDS:42d755054b10d6358ccbb1113cb407dc
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反应信息

  • 作为反应物:
    参考文献:
    名称:
    Thiazolopyrimidine modulators of TRPV1
    摘要:
    描述了某些调节TRPV1的噻唑吡咯啉化合物。这些化合物可以用于制备药物组合物和治疗由TRPV1活性介导的疾病状态、紊乱和病况的方法,如疼痛、关节炎、瘙痒、咳嗽、哮喘或炎症性肠病。
    公开号:
    US20080004253A1
  • 作为产物:
    描述:
    4,6-二氯-5-氨基嘧啶2,6-二甲基异硫氰酸苯酯caesium carbonate 作用下, 以 乙腈 为溶剂, 反应 16.0h, 以90%的产率得到(7-氯噻唑并[5,4-d]嘧啶-2-基)-(2,6-二甲基苯基)胺
    参考文献:
    名称:
    Single-Step Syntheses of 2-Amino-7-chlorothiazolo[5,4-d]pyrimidines:  Intermediates for Bivalent Thiazolopyrimidines
    摘要:
    A single-step process for the preparation of 2-amino-7-chlorothiazolo[5,4-d]pyrimidines, 2, was achieved by the reaction of the commercially available 4,6-dichloro-5-aminopyrimidine 1 with isothiocyanates. This mild reaction accommodates a variety of functionalized isothiocyanates and proceeds in good to excellent yields. The utility of such intermediates is exemplified by subsequent reaction with alkyl or arylamine nucleophiles to afford novel, differentially functionalized 2,7-diaminothiazolo[5,4-d]pyrimidines, 3.
    DOI:
    10.1021/jo0517702
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文献信息

  • Identification and synthesis of 2,7-diamino-thiazolo[5,4-d]pyrimidine derivatives as TRPV1 antagonists
    作者:Alec D. Lebsack、Bryan J. Branstetter、Michael D. Hack、Wei Xiao、Matthew L. Peterson、Nadia Nasser、Michael P. Maher、Hong Ao、Anindya Bhattacharya、Mena Kansagara、Brian P. Scott、Lin Luo、Raymond Rynberg、Michele Rizzolio、Sandra R. Chaplan、Alan D. Wickenden、J. Guy Breitenbucher
    DOI:10.1016/j.bmcl.2008.11.024
    日期:2009.1
    We have identified and synthesized a series of 2,7-diamino-thiazolo[5,4-d]pyrimidines as TRPV1 antagonists. An exploration of the structure-activity relationships at the 2-, 5-, and 7-positions of the thiazolo[5,4-d]pyrimidine led to the identification of several potent TRPV1 antagonists, including 3, 29, 51, and 57. Compound 3 was orally bioavailable and afforded a significant reversal of carrageenan-induced thermal hyperalgesia with an ED(50) = 0.5 mg/kg in rats. (C) 2008 Elsevier Ltd. All rights reserved.
  • THIAZOLOPYRIMIDINE MODULATORS OF TRPV1
    申请人:Janssen Pharmaceutica NV
    公开号:EP2044086A2
    公开(公告)日:2009-04-08
  • [EN] THIAZOLOPYRIMIDINE MODULATORS OF TRPV1<br/>[FR] MODULATEURS DE TRPV1 À BASE DE THIAZOLOPYRIMIDINE
    申请人:JANSSEN PHARMACEUTICA NV
    公开号:WO2008005303A2
    公开(公告)日:2008-01-10
    [EN] Certain TRPV1-modulating thiazolopyrimidine compounds are described. The compounds may be used in pharmaceutical compositions and methods for treating disease states, disorders, and conditions mediated by TRPV1 activity, such as pain, arthritis, itch, cough, asthma, or inflammatory bowel disease.
    [FR] La présente invention concerne certains composés de thiazolopyrimidine capables de moduler la protéine TRPV1. Les composés peuvent être utilisés dans des compositions pharmaceutiques et pour des procédés destinés au traitement d'états maladifs, de troubles, et de pathologies médiés par l'activité de la TRPV1, tels que la douleur, l'arthrite, le prurit, la toux, l'asthme, ou la maladie intestinale inflammatoire.
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同类化合物

噻唑并[5,4-d]嘧啶-7(4H)-酮 噻唑并[5,4-d]嘧啶-5,7(4H,6H)-二酮 噻唑并[5,4-d]嘧啶-2(1H)-酮 噻唑并[5,4-d]嘧啶,5-氯- 噻唑[5,4-D]嘧啶-2-胺 叔丁基-(7-氯噻唑并[5,4-d]嘧啶-2-基)-胺 [1,3]噻唑并[5,4-D]嘧啶-7-胺 N7-丁基-n2-苯基噻唑并[5,4-d]嘧啶-2,7-二胺 N7-(4-甲氧基苯基)-n2-苯基噻唑并[5,4-d]嘧啶-2,7-二胺 N7-(3-氯苯基)-n2-苯基噻唑并[5,4-d]嘧啶-2,7-二胺 N2-苯基-n7-(3,4,5-三甲氧基苄基)噻唑并[5,4-d]嘧啶-2,7-二胺 N2,N7-二苯基-噻唑并[5,4-d]嘧啶-2,7-二胺 N-(7-氯-2-甲基噻唑并[5,4-D]嘧啶-5-基)新戊酰胺 8-苯胺基-9-硫杂-2,4,7-三氮杂双环[4.3.0]壬-2,7,10-三烯-5-硫酮 7-氯噻唑并[5,4-D]嘧啶 7-氯-N-(邻甲苯基)噻唑并[5,4-D]嘧啶-2-胺 7-氯-5-甲基-[1,3]噻唑并[5,4-d]嘧啶 7-氯-5-(三氟甲基)[1,3]噻唑并[5,4-d]嘧啶 7-氨基-噻唑并[5,4-d]嘧啶-2(1H)-硫酮 7-(甲硫基)噻唑并[5,4-D]嘧啶-2-羧酸甲酯 5-甲硫基-9-硫杂-2,4,7-三氮杂双环[4.3.0]壬-2,4,7,10-四烯 5,7-二氯噻唑并[5,4-D]嘧啶 5,7-二氯-2-甲基-噻唑并[5,4-d]嘧啶 4-(5-氯噻唑并[5,4-D]嘧啶-7-基)吗啉 2-苯胺基[1,3]噻唑并[5,4-d]嘧啶-7-醇 2-苯基噻唑并[5,4-d]嘧啶-7-胺 2-甲基-4H-噻唑并[5,4-d]嘧啶-5,7-二酮 2-乙氧基[1,3]噻唑并[4,5-d]嘧啶-5,7(4H,6H)-二酮 2-(甲基硫代)-噻唑并[5,4-d]嘧啶-7(4H)-酮 2,7-二氯噻唑并[5,4-D]嘧啶 2,5-二氯噻唑并[5,4-d]嘧啶 2,5-二氨基-6H-[1,3]噻唑并[4,5-e]嘧啶-7-酮 1-(7-氯噻唑并[5,4-d]嘧啶-2-基)-1,3-二甲基硫脲 1,3-二苄基-1-(7-氯噻唑并[5,4-d]嘧啶-2-基)硫脲 (7-氯噻唑并[5,4-d]嘧啶-2-基)苯胺 (7-氯噻唑并[5,4-d]嘧啶-2-基)异丙胺 (7-氯噻唑并[5,4-d]嘧啶-2-基)-对甲苯-胺 (7-氯噻唑并[5,4-d]嘧啶-2-基)-吡啶-3-基-胺 (7-氯噻唑并[5,4-d]嘧啶-2-基)-(4-甲氧基苯基)胺 (7-氯噻唑并[5,4-d]嘧啶-2-基)-(2,6-二甲基苯基)胺 (6CI,7CI,8CI,9CI)-噻唑并[5,4-d]嘧啶 4-[7-methyl-4,6-dioxo-2-(3-phenyl-prop-1-ynyl)-6,7-dihydro-4H-1,4l4-dithia-3,5,7-triaza-inden-5-ylmethyl]-benzoic acid 7-Amino-2-methyl-5-hydroxy-thieno<3.2-g>pteridin 7-Amino-3-ethylmercapto-5-hydroxy-2-methyl-thieno<3.2-g>pteridin 2-(6-morpholin-4-yl-4H-[1,3]dithiino[5,4-d]pyrimidin-8-ylamino)-ethanol 2-ethoxycarbonylaminothiazolo[5,4-d]pyrimidine-7(6H)-one 7-chlorothiazolo[5,4-b]pyridine-2-carbonitrile 3-Brom-5-oxo-7-amino-2-(1,2-dihydroxyethyl)-thieno<3.2-g>pteridin 5-amino-2-(cyclohexyl)thiazolo[5,4-d]pyrimidine-7-thiol 5-amino-2-(2-furyl)-thiazolo[5,4-d]pyrimidine-7-thiol