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(RS)-3-(2-oxo-2,3-dihydro-1H-indol-5-yl-sulfanyl)-pyrrolidine-1-carboxylic acid tert-butyl ester | 371240-64-1

中文名称
——
中文别名
——
英文名称
(RS)-3-(2-oxo-2,3-dihydro-1H-indol-5-yl-sulfanyl)-pyrrolidine-1-carboxylic acid tert-butyl ester
英文别名
Tert-butyl 3-[(2-oxo-1,3-dihydroindol-5-yl)sulfanyl]pyrrolidine-1-carboxylate
(RS)-3-(2-oxo-2,3-dihydro-1H-indol-5-yl-sulfanyl)-pyrrolidine-1-carboxylic acid tert-butyl ester化学式
CAS
371240-64-1
化学式
C17H22N2O3S
mdl
——
分子量
334.439
InChiKey
BMLYGOAGGZEXGL-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):
    2.4
  • 重原子数:
    23
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    83.9
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • Heterocyclic compounds useful as NMDA receptor selective subtype blockers
    申请人:——
    公开号:US20010047031A1
    公开(公告)日:2001-11-29
    The invention relates to compounds of formula 1 wherein Ar 1 is pyridyl or phenyl, substituted by hydroxy, lower alkyl, halogen, amino, nitro, benzyloxy or lower alkoxy-lower alkoxy, or is the group 2 wherein Z 1 is a five membered heterocyclic ring, which contains one or two heteroatoms, selected from N or O; R 1 is hydrogen, hydroxy or an oxo group; Ar 2 is pyridyl or phenyl, optionally substituted by hydroxy, lower alkyl, halogen, amino, nitro, benzyloxy or lower alkoxy-lower alkoxy, or is the group 3 wherein Z 2 is a five or six membered ring, which optionally contains one or two heteroatoms, selected from N or O; and Q is —S—, —S(O)— or —S(O) 2 —; X is a bond, —CH(OH)— or —(CH 2 ) n —; A is a bond or —(CHR) m —; R is hydrogen, halogen or hydroxy, independently from each other if m is 2 or 3; Y is —(CR 2 ) m —, —O—, —C═C—, —C≡C—, piperidin- 1 -yl, pyrrolidin- 1 yl or C 4 -C 6 -cycloalkyl, which rings are optionally substituted by hydroxy; B is a bond, —O— or —(CHR) m ; n is 1 or 2; and m is 1 to 3 and pharmaceutically acceptable acid addition salts thereof with the exception of compounds, wherein A and B are simultaneously a bond and Y is —CHR—. The compounds may be used in the treatment of neurodegenerative diseases.
    该发明涉及具有以下结构的化合物:其中Ar1是吡啶基或苯基,被羟基、较低烷基、卤素、基、硝基、苄氧基或较低烷氧基取代,或者是基团2,其中Z1是一个含有一个或两个异原子(N或O)的五元杂环环,R1是氢、羟基或氧代基,Ar2是吡啶基或苯基,可选择地被羟基、较低烷基、卤素、基、硝基、苄氧基或较低烷氧基取代,或者是基团3,其中Z2是一个含有一个或两个异原子(N或O)的五元或六元环,Q是—S—、—S(O)—或—S(O)2—,X是一个键、—CH(OH)—或—(CH2)n—,A是一个键或—(CHR)m—,R是氢、卤素或羟基,如果m为2或3,则彼此独立,Y是—(CR2)m—、—O—、—C═C—、—C≡C—、哌啶-1-基、吡咯啉-1-基或C4-C6环烷基,这些环可选择地被羟基取代,B是一个键、—O—或—(CHR)m—,n为1或2,m为1到3,以及其与药学上可接受的酸盐,但除了A和B同时为键且Y为—CHR—的化合物。这些化合物可用于治疗神经退行性疾病。
  • PYRROLIDINE AND PIPERIDINE DERIVATIVES AND THEIR USE FOR THE TREATMENT OF NEURODEGENERATIVE DISORDERS
    申请人:F. HOFFMANN-LA ROCHE AG
    公开号:EP1278728B1
    公开(公告)日:2004-08-25
  • US6451819B2
    申请人:——
    公开号:US6451819B2
    公开(公告)日:2002-09-17
  • [EN] PYRROLIDINE AND PIPERIDINE DERIVATIVES AND THEIR USE FOR THE TREAMENT OF NEURODEGENERATIVE DISORDERS<br/>[FR] DERIVES DE LA PYRROLIDINE ET DE LA PIPERIDINE ET LEUR UTILISATION POUR LE TRAITEMENT DE MALADIES NEURODEGENERATIVES
    申请人:HOFFMANN LA ROCHE
    公开号:WO2001081303A1
    公开(公告)日:2001-11-01
    The invention relates to compounds of formula (I) wherein Ar1 is pyridyl or phenyl, substituted by hydroxy, lower alkyl, halogen, amino, nitro, benzyloxy or lower alkoxy-lower alkoxy, or is the group (a) wherein Z1 is a five membered heterocyclic ring, which contains one or two heteroatoms, selected from N or O; R1 is hydrogen, hydroxy or an oxo group; Ar2 is pyridyl or phenyl, optionally substituted by hydroxy, lower alkyl, halogen, amino, nitro, benzyloxy or lower alkoxy-lower alkoxy, or is the group (b) wherein Z2 is a five or six membered ring, which optionally contains one or two heteroatoms, selected from N or O; and Q is -S-, -S(O)- or -S(O)¿2?-; X is a bond, -CH(OH)- or -(CH2)n-; A is a bond or -(CHR)m-; R is hydrogen, halogen or hydroxy, independently from each other if m is 2 or 3; Y is -(CR2)m-, -O-, -C=C-, -C C-, piperidin-1-yl, pyrrolidin-1yl or C4-C6-cycloalkyl, which rings are optionally substituted by hydroxy; B is a bond, -O- or -(CHR)m; n is 1 or 2; and m is 1 to 3 and pharmaceutically acceptable acid addition salts thereof with the exception of compounds, wherein A and B are simultaneously a bond and Y is -CHR-. The compounds may be used in the treatment of neurodegenerative diseases.
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