Trifluoroacetic acid → 3-chloro-6-{1-[4-(cyclopropylsulfanyl)phenyl]-2-[(3R)-pyrrolidin-3-yl]ethenyl}-2-methoxypyridine

HRID 70619ノート

反応式

HRID 70619 の反応式
FC(F)(F)C(O)=O.[Cl:8][C:9]1[CH:10]=[CH:11][C:12]([C:17]([C:31]2[CH:36]=[CH:35][C:34]([S:37][CH:38]3[CH2:40][CH2:39]3)=[CH:33][CH:32]=2)=[CH:18][C@H:19]2[CH2:23][CH2:22][N:21](C(OC(C)(C)C)=O)[CH2:20]2)=[N:13][C:14]=1[O:15][CH3:16]>ClCCl>[Cl:8][C:9]1[C:14]([O:15][CH3:16])=[N:13][C:12]([C:17]([C:31]2[CH:32]=[CH:33][C:34]([S:37][CH:38]3[CH2:39][CH2:40]3)=[CH:35][CH:36]=2)=[CH:18][C@H:19]2[CH2:23][CH2:22][NH:21][CH2:20]2)=[CH:11][CH:10]=1

参加物

4

実験手順

Trifluoroacetic acid (1.5 mL) was added to a solution of tert-butyl (3R)-3-{2-(5-chloro-6-methoxypyridin-2-yl)-2-[4-(cyclopropylsulfanyl)phenyl]ethenyl}pyrrolidine-1-carboxylate (EZ mixture) (296 mg) in dichloromethane (3 mL) under ice-cooling, followed by stirring for three hours. The reaction solution was concentrated under reduced pressure to give 3-chloro-6-{1-[4-(cyclopropylsulfanyl)phenyl]-2-[(3R)-pyrrolidin-3-yl]ethenyl}-2-methoxypyridine (EZ mixture) as a crude product (235 mg).

後処理

  1. temperaturecooling
  2. concentrationThe reaction solution was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-4f44542ea77f41cda9b076698e676aad
出典データセット
uspto-grants-2014_09
特許番号
US08822503B2

反応ノート

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