Sodium Hydroxide → HCID 54452714、化合物
反応式
C([O:8][C:9](=[O:55])[C@H:10]([CH2:51][CH:52]([CH3:54])[CH3:53])[NH:11][C:12](=[O:50])[C@H:13]([CH2:43][C:44]1[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=1)[NH:14][C:15](=[O:42])[C@H:16]([CH3:41])[NH:17][C:18](=[O:40])[CH2:19][NH:20][C:21](=[O:39])[C@H:22]([CH2:31][C:32]1[CH:37]=[CH:36][C:35]([OH:38])=[CH:34][CH:33]=1)[NH:23][C:24]([O:26][C:27]([CH3:30])([CH3:29])[CH3:28])=[O:25])C1C=CC=CC=1.[OH-].[Na+]>CO>[C:27]([O:26][C:24]([NH:23][C@H:22]([C:21]([NH:20][CH2:19][C:18]([NH:17][C@H:16]([C:15]([NH:14][C@H:13]([C:12]([NH:11][C@H:10]([C:9]([OH:55])=[O:8])[CH2:51][CH:52]([CH3:53])[CH3:54])=[O:50])[CH2:43][C:44]1[CH:45]=[CH:46][CH:47]=[CH:48][CH:49]=1)=[O:42])[CH3:41])=[O:40])=[O:39])[CH2:31][C:32]1[CH:33]=[CH:34][C:35]([OH:38])=[CH:36][CH:37]=1)=[O:25])([CH3:28])([CH3:30])[CH3:29]参加物
4
反応条件
- 温度
- 10 °C
実験手順
18.9 Parts N-t-butoxycarbonyl-L-tyrosylglycyl-L-alanyl-L-phenylalanyl-L-leucine benzyl ester is dissolved in 70 parts methanol and the solution cooled to 10° C. Then, 90 parts by volume of a 1N sodium hydroxide solution is added dropwise with stirring while maintaining the temperature below 20° C. After standing at room temperature for 1 hour, the methanol is removed by evaporation under reduced pressure. The solution is washed once with ethyl ether to remove benzyl alcohol and the aqueous layer acidified with 90 parts by volume of a 1 N hydrochloric acid solution. The solid which results is filtered and washed with water to afford N-t-butoxycarbonyl-L-tyrosylglycyl-L-alanyl-L-phenylalanyl-L-leucine.
後処理
- temperaturewhile maintaining the temperature below 20° C
- customthe methanol is removed by evaporation under reduced pressure
- washThe solution is washed once with ethyl ether
- customto remove benzyl alcohol
- customThe solid which results
- filtrationis filtered
- washwashed with water
出典と根拠
- ORDレコード
- ord-a25e1183125f44359966c2df80989f8c
- 出典データセット
- uspto-grants-1977_06
- 特許番号
- US04028319
反応ノート
読み込み中…