Hydrochloric Acid → 3-Methoxy-4-phenylaminopyrrolidine hydrochloride
反応式
C(OC([N:8]1[CH2:12][CH:11]([NH:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:10]([O:20][CH3:21])[CH2:9]1)=O)(C)(C)C.[ClH:22]>CO>[ClH:22].[CH3:21][O:20][CH:10]1[CH:11]([NH:13][C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH2:12][NH:8][CH2:9]1参加物
4
実験手順
In 100 ml of methanol was dissolved 1.98 g (0.0068 mole) of 1-t-butoxycarbonyl-3-methoxy-4-phenylaminopyrrolidine obtained as described above, and 23.5 ml of 6N hydrochloric acid was added thereto. The mixture was left to stand at room temperature overnight. The solvent was removed under reduced pressure, and the residue was washed with ethanol to obtain 1.71 g of 3-methoxy-4-phenylaminopyrrolidine hydrochloride as white powder.
後処理
- customobtained
- additionwas added
- waitThe mixture was left
- customThe solvent was removed under reduced pressure
- washthe residue was washed with ethanol
出典と根拠
- ORDレコード
- ord-777e9efddb904059b9ce049d57098e4f
- 出典データセット
- uspto-grants-1996_05
- 特許番号
- US05519016
反応ノート
読み込み中…