Hydrochloric Acid → (5-(R)-(4-aminomethylphenyl)-2,4-dioxoimidazolidin-3-yl)acetic acid hydrochloride
反応式
C(OC([NH:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([C@@H:19]([NH:24][C:25]([NH:27][CH2:28][C:29]([O:31]CC)=[O:30])=[O:26])[C:20](OC)=[O:21])=[CH:15][CH:14]=1)=O)C1C=CC=CC=1.[ClH:34]>>[ClH:34].[NH2:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([C@H:19]2[NH:24][C:25](=[O:26])[N:27]([CH2:28][C:29]([OH:31])=[O:30])[C:20]2=[O:21])=[CH:15][CH:14]=1参加物
3
実験手順
280 mg of N-(1-(R)-(4-benzyloxycarbonylaminomethylphenyl-1-methoxycarbonylmethyl),N'-ethoxycarbonylmethylurea are boiled under reflux for 45 min in 4 ml of 6N HCl and the mixture is then concentrated and dried over KOH.
後処理
- concentrationthe mixture is then concentrated
- dry with materialdried over KOH
出典と根拠
- ORDレコード
- ord-5768d5e45d17463e94180f69eeb44af0
- 出典データセット
- uspto-grants-1995_06
- 特許番号
- US05424293
反応ノート
読み込み中…