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4'-(bromomethyl)-3'-fluorobiphenyl-2-carbonitrile | 136042-63-2

中文名称
——
中文别名
——
英文名称
4'-(bromomethyl)-3'-fluorobiphenyl-2-carbonitrile
英文别名
2-[4-(bromomethyl)-3-fluorophenyl]benzonitrile
4'-(bromomethyl)-3'-fluorobiphenyl-2-carbonitrile化学式
CAS
136042-63-2
化学式
C14H9BrFN
mdl
——
分子量
290.135
InChiKey
NJPYERBPKMGOCR-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):
    3.9
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    23.8
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-butyl-6-methylpyrimidin-4(3H)-one4'-(bromomethyl)-3'-fluorobiphenyl-2-carbonitrilepotassium carbonate 作用下, 以 乙腈 为溶剂, 反应 12.0h, 以29%的产率得到4'-[(2-butyl-4-methyl-6-oxopyrimidin-1(6H)-yl)methyl]-3'-fluorobiphenyl-2-carbonitrile
    参考文献:
    名称:
    WO2008/62905
    摘要:
    公开号:
  • 作为产物:
    描述:
    2-(3-Fluoro-4-methylphenyl)-benzonitrileN-溴代丁二酰亚胺(NBS)三氟甲苯偶氮二异丁腈三氟甲苯 作用下, 反应 16.0h, 以to give a solution of 4′-(bromomethyl)-3′-fluorobiphenyl-2-carbonitrile in benzotrifluoride的产率得到4'-(bromomethyl)-3'-fluorobiphenyl-2-carbonitrile
    参考文献:
    名称:
    Fused ring compound and use thereof
    摘要:
    提供的是一种新型化合物,其化学式如下所示,其中每个符号均如规范中定义,或其盐,其具有血管紧张素II受体拮抗活性和过氧化物酶体增殖物激活受体γ激动活性,并可用作预防或治疗循环系统疾病,如高血压等,代谢性疾病,如糖尿病等的药物。
    公开号:
    US09115136B2
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文献信息

  • FUSED RING COMPOUND AND USE THEREOF
    申请人:Maekawa Tsuyoshi
    公开号:US20100197683A1
    公开(公告)日:2010-08-05
    Provided is a novel compound represented by the following formula Wherein each symbol is as defined in the specification, or a salt thereof, which has an angiotensin II receptor antagonistic activity and a peroxisome proliferator-activated receptor γ agonistic activity, and is useful as an agent for the prophylaxis or treatment of circulatory diseases such as hypertension and the like and/or metabolic diseases such as diabetes and the like, and the like.
    提供的是一种新化合物,其化学式如下所示。其中每个符号如规范中定义,或其盐,具有抗肾素II受体拮抗活性和过氧化物酶增殖激活受体γ激动活性,可用作预防或治疗循环疾病(如高血压等)和/或代谢疾病(如糖尿病等)的药物。
  • HETEROMONOCYCLIC COMPOUND AND USE THEREOF
    申请人:Kuroita Takanobu
    公开号:US20080207654A1
    公开(公告)日:2008-08-28
    A compound represented by the formula (I): wherein R1 is an oxo group, ═N—R or the like; a group represented by the formula: is a group represented by the formula: R2 is a group represented by the formula: R3 and R4 are each H, or C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 alkoxy, C1-C6 alkylamino, di(C1-C6)alkylamino or C1-C6 alkylthio, each of which is optionally substituted; and R5 is H, or C1-C6 alkyl, C2-C6 alkenyl, cyclic group, each of which is optionally substituted, —CO—R8 or —O—R8′, or a salt thereof. The compound of the present invention is useful as a drug for the prophylaxis or treatment of circulatory diseases, metabolic diseases and/or central nervous system diseases.
    化合物的化学式为(I),其中R1为氧代基,═N—R或类似基团;式中的基团表示为:其中R2为式中的基团;R3和R4分别为H,或C1-C6烷基,C3-C6环烷基,C1-C6烷氧基,C1-C6烷基氨基,二(C1-C6)烷基氨基或C1-C6烷基硫基,每个基团均可选地被取代;R5为H,或C1-C6烷基,C2-C6烯基,环状基团,每个基团均可选地被取代,—CO—R8或—O—R8′,或其盐。本发明的化合物可用作预防或治疗循环系统疾病、代谢性疾病和/或中枢神经系统疾病的药物。
  • HETEROCYCLIC COMPOUND AND USE THEREOF
    申请人:Kuroita Takanobu
    公开号:US20100137281A1
    公开(公告)日:2010-06-03
    The present invention aims to provide a compound having superior pharmacological action, physicochemical properties and the like, which is useful for the prophylaxis or treatment s of circulatory diseases such as hypertension, cardiac diseases, arteriosclerosis, renal diseases, cerebral apoplexy and the like and/or metabolic diseases such as hyperlipidemia, obesity, diabetes and the like, central nervous disorders such as cerebral infarction and the like, mental diseases such as dementia, depression and the like, and the like. A compound represented by the formula (I): wherein each symbol is as defined in the specification, or a salt thereof.
    本发明旨在提供一种具有优异的药理作用、物理化学性质等的化合物,该化合物对预防或治疗循环系统疾病,如高血压、心脏疾病、动脉硬化、肾脏疾病、脑卒中等,和/或代谢性疾病,如高脂血症、肥胖、糖尿病等,中枢神经系统疾病,如脑梗死等,精神疾病,如痴呆、抑郁症等,等方面具有用途。该化合物由式(I)所表示,其中每个符号如规范中所定义,或其盐。
  • Substituted pyrimidines and [1,2, 4] triazoles and the use thereof for treating prophylaxis, cardiovascular diseases, metabolic diseases and/or central nervous system diseases
    申请人:Takeda Pharmaceutical Company Limited
    公开号:US07998968B2
    公开(公告)日:2011-08-16
    A compound represented by the formula (I): wherein R1 is an oxo group, ═N—R or the like; a group represented by the formula: is a group represented by the formula: R2 is a group represented by the formula: R3 and R4 are each H, or C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 alkoxy, C1-C6 alkylamino, di(C1-C6)alkylamino or C1-C6 alkylthio, each of which is optionally substituted; and R5 is H, or C1-C6 alkyl, C2-C6 alkenyl, cyclic group, each of which is optionally substituted, —CO—R8 or —O—R8′, or a salt thereof. For example, the compound may be substituted pyrimidines and pharmaceutical compositions of the formula (I) where X=—CR3; X1=—CR2 or —NR2; and X2=—CR5 or —NR5. The compound of the present invention is useful as a drug for the prophylaxis or treatment of cardiovascular diseases, metabolic diseases and/or central nervous system diseases.
    化合物的化学式为(I):其中R1是氧代基,═N—R或类似的基团;由式子表示的基团:是由式子表示的基团:R2是由式子表示的基团:R3和R4分别是H,或C1-C6烷基,C3-C6环烷基,C1-C6烷氧基,C1-C6烷基氨基,二(C1-C6)烷基氨基或C1-C6烷基硫基,每个基团都可以选择性地被取代;而R5是H,或C1-C6烷基,C2-C6烯基,环状基团,每个基团都可以选择性地被取代,—CO—R8或—O—R8′,或其盐。例如,该化合物可以是取代的嘧啶,并且具有化学式(I)的制药组合物,其中X=—CR3;X1=—CR2或—NR2;X2=—CR5或—NR5。本发明的化合物可用作预防或治疗心血管疾病、代谢性疾病和/或中枢神经系统疾病的药物。
  • Heteromonocyclic compound or a salt thereof having strong antihypertensive action, insulin sensitizing activity and the like production thereof and use thereof for prophylaxis or treatment of cardiovascular diseases, metabolic diseases and/or central nervous system diseases
    申请人:Takeda Pharmaceutical Company Limited
    公开号:US07803940B2
    公开(公告)日:2010-09-28
    A compound represented by the formula (I): wherein R1 is an oxo group, ═N—R or the like; a group represented by the formula: is a group represented by the formula: R2 is a group represented by the formula: R3 and R4 are each H, or C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 alkoxy, C1-C6 alkylamino, di(C1-C6)alkylamino or C1-C6 alkylthio, each of which is optionally substituted; and R5 is H, or C1-C6 alkyl, C2-C6 alkenyl, cyclic group, each of which is optionally substituted, —CO—R8 or —O—R8′, or a salt thereof. The compound of the present invention is useful as a drug for the prophylaxis or treatment of cardiovascular diseases, metabolic diseases and/or central nervous system diseases.
    化合物的化学式为(I),其中R1代表氧代基,═N—R或类似基团;式中代表的基团为:R2代表式中代表的基团;R3和R4分别代表氢、C1-C6烷基、C3-C6环烷基、C1-C6烷氧基、C1-C6烷基氨基、双(C1-C6)烷基氨基或C1-C6烷基硫基,每个基团都可以选择性地被取代;R5代表氢、C1-C6烷基、C2-C6烯基、环状基团,每个基团都可以选择性地被取代,—CO—R8或—O—R8′,或其盐。本发明的化合物可用作预防或治疗心血管疾病、代谢性疾病和/或中枢神经系统疾病的药物。
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