(2S,3S)-2-Phenyl-3-(5-(2,2,2-trifluoro-1-(trifluoromethyl)ethyl)-2-methoxybenzyl)aminopiperidine → (2S,3S)-2-Phenyl-3-(5-(2,2,2-trifluoro-1-(trifluoromethyl)ethyl)-2-methoxybenzyl)aminopiperidine dihydrochloride

HRID 1634325ノート

反応式

HRID 1634325 の反応式
[C:1]1([C@H:7]2[C@@H:12]([NH:13][CH2:14][C:15]3[CH:20]=[C:19]([CH:21]([C:26]([F:29])([F:28])[F:27])[C:22]([F:25])([F:24])[F:23])[CH:18]=[CH:17][C:16]=3[O:30][CH3:31])[CH2:11][CH2:10][CH2:9][NH:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[ClH:32].CO>C(Cl)Cl>[ClH:32].[ClH:32].[C:1]1([C@H:7]2[C@@H:12]([NH:13][CH2:14][C:15]3[CH:20]=[C:19]([CH:21]([C:26]([F:27])([F:28])[F:29])[C:22]([F:23])([F:24])[F:25])[CH:18]=[CH:17][C:16]=3[O:30][CH3:31])[CH2:11][CH2:10][CH2:9][NH:8]2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

参加物

4

実験手順

To a solution of Compound 14 (160 mg) in CH2Cl2 (10 ml) was added an excess amount of 10% HCl-MeOH (6 ml). After the solvent was evaporated in vacuo, the residual solid was recrystallized from IPA to give Compound 15 (130 mg, 83%; three steps) as a colorless crystal.

後処理

  1. customAfter the solvent was evaporated in vacuo
  2. customthe residual solid was recrystallized from IPA

出典と根拠

ORDレコード
ord-42215b84c70043efb3a643bffcf099cc
出典データセット
uspto-grants-2003_01
特許番号
US06506775B1

反応ノート

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