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(S)-3-((2,2-dimethyl-1,3-dioxacyclopent-4-yl)methoxy)-4-methyl-1-phenyl-1H-pyrazol-5-ylaminocarboxylic acid phenyl ester | 1414581-36-4

中文名称
——
中文别名
——
英文名称
(S)-3-((2,2-dimethyl-1,3-dioxacyclopent-4-yl)methoxy)-4-methyl-1-phenyl-1H-pyrazol-5-ylaminocarboxylic acid phenyl ester
英文别名
(S)-3-((2,2-dimethyl-1,3-dioxacyclopentane-4-yl)methoxy)-4-methyl-1-phenyl-1H-pyrazol-5-ylcarbamic acid phenyl ester;(S)-3-((2,2-dimethyl-1,3-dioxacyclopent-4-yl)methoxy)-4-methyl-1-phenyl-1H-pyrazol-5-ylcarbamic acid phenyl ester;(S)-phenyl 3-((2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)-4-methyl-1-phenyl-1H-pyrazol-5-ylcarbamate;phenyl N-[5-[[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]methoxy]-4-methyl-2-phenylpyrazol-3-yl]carbamate
(S)-3-((2,2-dimethyl-1,3-dioxacyclopent-4-yl)methoxy)-4-methyl-1-phenyl-1H-pyrazol-5-ylaminocarboxylic acid phenyl ester化学式
CAS
1414581-36-4
化学式
C23H25N3O5
mdl
——
分子量
423.469
InChiKey
AXABFBJHFXZJSA-IBGZPJMESA-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):
    4.3
  • 重原子数:
    31
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    83.8
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    8-methyl-2-phenylimidazo[1,2-a]pyridin-3-amine dihydrochloride 、 (S)-3-((2,2-dimethyl-1,3-dioxacyclopent-4-yl)methoxy)-4-methyl-1-phenyl-1H-pyrazol-5-ylaminocarboxylic acid phenyl esterN,N-二异丙基乙胺 作用下, 以 N,N-二甲基乙酰胺 为溶剂, 反应 16.0h, 以93%的产率得到(S)-1-(3-((2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)-4-methyl-1-phenyl-1H-pyrazol-5-yl)-3-(8-methyl-2-phenylimidazo[1,2-a]pyridin-3-yl)urea
    参考文献:
    名称:
    [EN] BICYCLIC HETEROARYL UREA, THIOUREA, GUANIDINE AND CYANOGUANIDINE COMPOUNDS AS TRKA KINASE INHIBITORS
    [FR] COMPOSÉS D'HÉTÉROARYLE URÉE, THIOURÉE,GUANIDINE ET CYANOGUANIDINE EN TANT QU'INHIBITEURS DE LA KINASE TRKA
    摘要:
    式I化合物或其立体异构体、互变异构体或药学上可接受的盐、溶剂合物或前药,其中环A、环C和X如本文所定义,是TrkA激酶的抑制剂,并且在治疗可以用TrkA激酶抑制剂治疗的疾病中具有用处,如疼痛、癌症、炎症/炎症性疾病、神经退行性疾病、某些传染病、干燥综合征、子宫内膜异位症、糖尿病周围神经病变、前列腺炎和盆腔疼痛综合征。
    公开号:
    WO2014078408A1
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文献信息

  • PYRROLIDINYL UREA, PYRROLIDINYL THIOUREA AND PYRROLIDINYL GUANIDINE COMPOUNDS AS TRKA KINASE INHIBITORS
    申请人:Allen Shelley
    公开号:US20150166564A1
    公开(公告)日:2015-06-18
    Compounds of Formula I: or stereoisomers, tautomers, or pharmaceutically acceptable salts, or solvates or prodrugs thereof, where R 1 , R 2 , R a , R b , R c , R d , X, Y, B, and Ring C are as defined herein, and wherein the Y—B moiety and the NH—C(═X)—NH moiety are in the trans configuration, are inhibitors of TrkA kinase and are useful in the treatment of diseases which can be treated with a TrkA kinase inhibitor such as pain, cancer, inflammation, neurodegenerative diseases and certain infectious diseases.
    化合物I的公式:或其立体异构体、互变异构体、药学上可接受的盐、溶剂或前药,其中R1、R2、Ra、Rb、Rc、Rd、X、Y、B和环C的定义如本文所述,其中Y-B基团和NH-C(═X)-NH基团处于反式构象,是TrkA激酶的抑制剂,可用于治疗可以通过TrkA激酶抑制剂治疗的疾病,例如疼痛、癌症、炎症、神经退行性疾病和某些传染病。
  • Pyrrolidinyl urea, pyrrolidinyl thiourea and pyrrolidinyl guanidine compounds as TrkA kinase inhibitors
    申请人:Array BioPharma Inc.
    公开号:US10323022B2
    公开(公告)日:2019-06-18
    Compounds of Formula I: or stereoisomers, tautomers, or pharmaceutically acceptable salts, or solvates or prodrugs thereof, where R1, R2, Ra, Rb, Rc, Rd, X, Y, B, and Ring C are as defined herein, and wherein the Y—B moiety and the NH—C(═X)—NH moiety are in the trans configuration, are inhibitors of TrkA kinase and are useful in the treatment of diseases which can be treated with a TrkA kinase inhibitor such as pain, cancer, inflammation, neurodegenerative diseases and certain infectious diseases.
    式 I 的化合物: 或其立体异构体、同系物、或其药学上可接受的盐、或其溶剂或原药,其中 R1、R2、Ra、Rb、Rc、Rd、X、Y、B 和环 C 如本文所定义,且其中 Y-B 分子和 NH-C(═X)-NH 分子为反式构型、是 TrkA 激酶的抑制剂,可用于治疗可使用 TrkA 激酶抑制剂治疗的疾病,如疼痛、癌症、炎症、神经退行性疾病和某些传染性疾病。
  • PYRROLIDINYL UREA, PYRROLIDINYL THIOUREA AND PYRROLIDINYL GUANIDINE COMPOUNDS AS TRKA KINASE INHIBITORS
    申请人:Array Biopharma, Inc.
    公开号:EP2712358B1
    公开(公告)日:2016-12-21
  • BICYCLIC HETEROARYL UREA, THIOUREA, GUANIDINE AND CYANOGUANIDINE COMPOUNDS AS TRKA KINASE INHIBITORS
    申请人:ARRAY BIOPHARMA INC.
    公开号:US20160355517A1
    公开(公告)日:2016-12-08
    Compounds of Formula I or stereoisomers, tautomers, or pharmaceutically acceptable salts, solvates or prodrugs thereof, wherein Ring A, Ring C and X are as defined herein, are inhibitors of TrkA kinase and are useful in the treatment of diseases which can be treated with a TrkA kinase inhibitor such as pain, cancer, inflammation/inflammatory diseases, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis and pelvic pain syndrome.
  • US9562055B2
    申请人:——
    公开号:US9562055B2
    公开(公告)日:2017-02-07
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