反応式
[CH3:1][O:2][C:3](=[O:15])[C@H:4]([CH3:14])[NH:5][C:6]1[CH:11]=[CH:10][C:9]([Cl:12])=[C:8]([Cl:13])[CH:7]=1.[CH3:16][CH:17]([CH3:22])[CH2:18][CH2:19]CO>>[CH3:16][CH:17]([CH3:22])[CH2:18][CH2:19][CH2:1][O:2][C:3](=[O:15])[C@H:4]([CH3:14])[NH:5][C:6]1[CH:11]=[CH:10][C:9]([Cl:12])=[C:8]([Cl:13])[CH:7]=1参加物
3
実験手順
Following transesterification General Procedure AB above and using N-(3,4-dichlorophenyl)alanine methyl ester (from Example A9 above) and 4-methylpentanol (Aldrich), the title compound was prepared as an oil. The reaction was monitored by silica gel tlc (Rf=0.70 in 25% EtOAc/hexanes). Purification was by preparative plate chromatography (silica gel using 25% EtOAc/hexanes as the eluant).
後処理
- customPurification
出典と根拠
- ORDレコード
- ord-49fd3b851c84444f9759642fd5a57715
- 出典データセット
- uspto-grants-2008_06
- 特許番号
- US07390801B2
関連ノート
読み込み中…