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6-cyclopropylmethoxy-4-hydroxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tertbutyl ester | 1692950-02-9

中文名称
——
中文别名
——
英文名称
6-cyclopropylmethoxy-4-hydroxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tertbutyl ester
英文别名
tert-butyl 6-(cyclopropylmethoxy)-4-hydroxy-3,4-dihydroisoquinoline-2(1H)-carboxylate;6-Cyclopropylmethoxy-4-hydroxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester;tert-butyl 6-(cyclopropylmethoxy)-4-hydroxy-3,4-dihydro-1H-isoquinoline-2-carboxylate
6-cyclopropylmethoxy-4-hydroxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tertbutyl ester化学式
CAS
1692950-02-9
化学式
C18H25NO4
mdl
——
分子量
319.401
InChiKey
FVFWHEAKNFTZCM-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):
    2.2
  • 重原子数:
    23
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.61
  • 拓扑面积:
    59
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • T-TYPE CALCIUM CHANNEL BLOCKER
    申请人:Nissan Chemical Industries, Ltd.
    公开号:EP3053917A1
    公开(公告)日:2016-08-10
    It is an object to provid a novel compound that has an excellent T-type calcium channel inhibitory activity and is specifically useful for prevention or treatment of pain, chronic kidney disease and atrial fibrillation. The present invention provides a novel triazinone compound of Formula (I): where each substituent in the formula is defined in detail in the description, and R1 means a hydrogen atom, or a C1-6 alkyl group, etc., E means a 7 to 14-membered non-aromatic fused heterocyclic group, L3 means a C1-6 alkylene group, etc., D means a C6-14 aryyl group or a 5 to 10-membered heteroaryl group each of which is optionally substituted, etc., a tautomer of the compound, or a pharmaceutically acceptable salt thereof, or a solvate thereof.
    本发明提供一种新颖的化合物,具有优异的T型通道抑制活性,特别适用于预防或治疗疼痛、慢性肾脏疾病和心房颤动。该新颖的三氮杂酮化合物的化学式如下(I):其中公式中的每个取代基在描述中有详细定义,R1表示氢原子,或者C1-6烷基等,E表示一个由非芳香性融合杂环组成的7到14成员环,L3表示C1-6烷基链等,D表示一个C6-14芳基或者一个5到10成员杂环基,每个基都可以选择性取代等,化合物的互变异构体,或其药学上可接受的盐,或其溶剂化合物。
  • T-TYPE CALCIUM CHANNEL INHIBITOR
    申请人:NISSAN CHEMICAL INDUSTRIES, LTD.
    公开号:US20160237071A1
    公开(公告)日:2016-08-18
    A novel compound that has an excellent T-type calcium channel inhibitory activity and is specifically useful for prevention or treatment of pain, chronic kidney disease and atrial fibrillation. The novel triazinone compound of Formula (I): where each substituent in the formula is defined in detail in the description, and R 1 could be a hydrogen atom, or a C 1-6 alkyl group, etc., E could be a 7 to 14-membered non-aromatic fused heterocyclic group, L 3 could be a C 1-6 alkylene group, etc., D could be a C 6-14 aryl group or a 5 to 10-membered heteroaryl group each of which is optionally substituted, etc., a tautomer of the compound, or a pharmaceutically acceptable salt thereof, or a solvate thereof.
    一种新型化合物,具有出色的T型通道抑制活性,特别适用于预防或治疗疼痛、慢性肾脏疾病和心房颤动。该新型三嗪酮化合物的化学式为(I),其中公式中的每个取代基在描述中都有详细定义,R1可以是氢原子或C1-6烷基等,E可以是7-14个成员的非芳香融合杂环基,L3可以是C1-6亚烷基等,D可以是C6-14芳基或5-10个成员的杂环芳基,每个基团都可以有选择性地取代等,该化合物的互变异构体或药学上可接受的盐或溶剂化物。
  • Tetrahydroisoquinoline derivatives, pharmaceutical compositions and uses thereof
    申请人:Boehringer Ingelheim International GmbH
    公开号:US09340510B2
    公开(公告)日:2016-05-17
    The invention relates to new pyrrolidine derivatives of the formula wherein R1 to R6, n and m are as defined in the description and claims, to their use as medicaments, to methods for their therapeutic use and to pharmaceutical compositions containing them.
    本发明涉及新的吡咯烷衍生物,其化学式为其中R1至R6,n和m如说明书和权利要求所定义,以及它们作为药物的用途,它们的治疗用途的方法以及含有它们的制药组合物。
  • TETRAHYDROISOQUINOLINE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS USEFUL FOR THE TREATMENT OF OBESITY AND DIABETES
    申请人:Boehringer Ingelheim International GmbH
    公开号:EP3194367B1
    公开(公告)日:2021-08-18
  • US9340510B2
    申请人:——
    公开号:US9340510B2
    公开(公告)日:2016-05-17
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