1,4-dimethylpyrrolidine-2-carboxylic acid | 89921-40-4

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 1,4-dimethylpyrrolidine-2-carboxylic acid
• 英文别名: γ-Methyl-N-methylprolin
• CAS: 89921-40-4
• 化学式: C₇H₁₃NO₂
• mdl: MFCD19230078
• 分子量: 143.186
• InChiKey: FAKNQOZVXKYTPZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1.5
• 重原子数：
  10
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.857
• 拓扑面积：
  40.5
• 氢给体数：
  1
• 氢受体数：
  3

文献信息

• SUBSTITUTED PYRROLIDINES AS FACTOR XIA INHIBITORS FOR THE TREATMENT THROMBOEMBOLIC DISEASES
  申请人：Imagawa Akira

  公开号：US20150152048A1

  公开（公告）日：2015-06-04

  The present invention provides compounds of the general formula (I), their salts and N-oxides, and solvates and prodrugs thereof (wherein the substituents are as defined in the description). The compounds of the general formula (I) are inhibitors of factor XIa, and are useful in the prevention of and/or therapy for thromboembolic diseases.

  本发明提供了一般式(I)的化合物，及其盐和N-氧化物，以及它们的溶剂合物和前药（其中取代基如描述中定义）。一般式(I)的化合物是因子XIa的抑制剂，并且在预防和/或治疗血栓栓塞疾病方面具有用途。
• Compounds, Compositions and Methods
  申请人：Morgan Bradley P.

  公开号：US20090324511A1

  公开（公告）日：2009-12-31

  Certain substituted urea derivatives selectively modulate the cardiac sarcomere, for example by potentiating cardiac myosin, and are useful in the treatment of systolic heart failure including congestive heart failure.

  某些取代脲衍生物可以选择性地调节心脏肌节，例如通过增强心肌肌球蛋白，对于治疗包括充血性心力衰竭在内的收缩期心力衰竭非常有用。
• MACROCYLIC INHIBITORS OF HEPATITIS C VIRUS
  申请人：Simmen Kenneth Alan

  公开号：US20090247512A1

  公开（公告）日：2009-10-01

  Inhibitors of HCV replication of formula (I) and the N-oxides, salts, or stereoisomers thereof, wherein each dashed line represents an optional double bond; X is N, CH and where X bears a double bond it is C; R 1 is —OR 6 , —NH—SO 2 R 7 ; R 2 is hydrogen, and where X is C or CH, R 2 may also be C 1-6 alkyl; R 3 is hydrogen, C 1-6 alkyl, C 1-6 alkoxyC 1-6 alkyl, or C 3-7 cycloalkyl; n is 3, 4, 5, or 6; R 4 and R 5 taken together with the nitrogen atom to which they are attached form a bicyclic ring system selected from wherein said ring system may optionally be substituted with 1-3 substituents; R 6 is hydrogen; aryl; Het; C 3-7 cycloalkyl optionally substituted with C 1-6 alkyl; or C 1-6 alkyl optionally substituted with C 3-7 cycloalkyl, aryl or with Het; R 7 is aryl; Het; C 3-7 cycloalkyl optionally substituted with C 1-6 alkyl; or C 1-6 alkyl optionally substituted with C 3-7 cycloalkyl, aryl or with Het; aryl is phenyl or naphthyl, each of which may be optionally substituted with 1-3 substituents; Het is a 5 or 6 membered saturated, partially unsaturated or completely unsaturated heterocyclic ring containing 1 to 4 heteroatoms each independently selected from N, O or S, and being optionally substituted with 1-3 substituents pharmaceutical compositions containing compounds (I) and processes for preparing compounds (I). Bioavailable combinations of the inhibitors of HCV of formula (I) with ritonavir are also provided.

  HCV复制抑制剂的公式（I）及其N-氧化物，盐或立体异构体，其中每个虚线表示可选的双键；X为N，CH，其中X带有双键时为C；R1为—OR6，—NH—SO2R7；R2为氢，其中X为C或CH时，R2也可以是C1-6烷基；R3为氢，C1-6烷基，C1-6烷氧基C1-6烷基或C3-7环烷基；n为3、4、5或6；R4和R5与它们所连接的氮原子共同形成选自下列的双环系统，其中所述环系统可以选择性地被1-3个取代基取代；R6为氢；芳基；Het；C3-7环烷基，可选地取代C1-6烷基；或C1-6烷基，可选地取代C3-7环烷基，芳基或与Het取代基；R7为芳基；Het；C3-7环烷基，可选地取代C1-6烷基；或C1-6烷基，可选地取代C3-7环烷基，芳基或与Het取代基；芳基为苯基或萘基，每个都可以选择性地被1-3个取代基取代；Het是一个含有1-4个杂原子的5或6元饱和、部分不饱和或完全不饱和的杂环，每个杂原子独立地选自N、O或S，并且可以选择性地被1-3个取代基取代。本发明还提供含有化合物（I）的制药组合物和制备化合物（I）的方法。公式（I）的HCV抑制剂与利托那韦的生物利用度组合也提供。
• MACROCYCLIC INHIBITORS OF HEPATITIS C VIRUS
  申请人：Raboisson Pierre Jean-Marie

  公开号：US20100022578A1

  公开（公告）日：2010-01-28

  Inhibitors of HCV replication of formula (I) and the salts and stereoisomers thereof, wherein each dashed line (represented by represents an optional double bond; X is N, CH and where X bears a double bond it is C; R 1 is —OR 7 , —NH—SO 2 R 8 ; R 2 is hydrogen, and where X is C or CH, R 2 may also be C 1-6 alkyl; R 3 is hydrogen, C 1-6 alkyl, C 1-6 alkoxyC 1-6 alkyl, C 3-7 cycloalkyl; n is 3, 4, 5, or 6; R 4 is C 1-6 alkyl or C 3-7 cycloalkyl; R 5 is hydrogen, halo, C 1-6 alkyl, hydroxy, C 1-6 alkoxy, polyhaloC 1-6 alkyl; R 6 is hydrogen, C 1-6 alkoxy, mono- or diC 1-6 alkylamino; or R 5 and R 6 may form a 5- or 6-membered unsaturated or partially unsaturated ring, optionally comprising one or two selected from O, N and S; R 7 is hydrogen; C 3-7 cycloalkyl optionally substituted with C 1-6 alkyl; or C 1-6 alkyl optionally substituted with C 3-7 cycloalkyl; R 8 is C 3-7 cycloalkyl optionally substituted with C 1-6 alkyl; C 1-6 alkyl optionally substituted with C 3-7 cycloalkyl; or —NR 8a R 8b ; R 8a and R 8b are C 1-6 alkyl, or both may form a 5- or 6-membered saturated heterocyclic ring; pharmaceutical compositions containing compounds (I) and processes for preparing compounds (I).

  公式（I）及其盐和立体异构体的HCV复制抑制剂，其中每个虚线（由表示可选双键）; X为N，CH，其中X带有双键时为C; R1为—OR7，—NH—SO2R8; R2为氢，当X为C或CH时，R2也可以是C1-6烷基; R3为氢，C1-6烷基，C1-6烷氧基C1-6烷基，C3-7环烷基; n为3、4、5或6; R4为C1-6烷基或C3-7环烷基; R5为氢，卤素，C1-6烷基，羟基，C1-6烷氧基，多卤素C1-6烷基; R6为氢，C1-6烷氧基，单烷基或二烷基氨基; 或R5和R6可以形成一个5-或6-成员的不饱和或部分不饱和环，可选地包括O、N和S中的一个或两个; R7为氢; C3-7环烷基，可选地被C1-6烷基取代; 或C1-6烷基，可选地被C3-7环烷基取代; R8为C3-7环烷基，可选地被C1-6烷基取代; C1-6烷基，可选地被C3-7环烷基取代; 或—NR8aR8b; R8a和R8b为C1-6烷基，或两者可以形成一个5-或6-成员的饱和杂环; 包含化合物（I）的制药组合物和制备化合物（I）的方法。
• Macrocylic Inhibitors of Hepatitis C Virus
  申请人：Simmen Kenneth Alan

  公开号：US20080262058A1

  公开（公告）日：2008-10-23

  Inhibitors of HCV replication of formula (I) wherein W is a heterocycle of formula and the remaining variables are as defined in the specification.

  HCV复制抑制剂的公式（I），其中W是公式的杂环，其余变量如规范中所定义。