反応式
[CH2:1]([O:3][C:4]([C:6]1[CH2:11][C@H:10]([NH2:12])[C@@H:9]([NH:13][C:14](=[O:16])[CH3:15])[C@H:8]([O:17][CH:18]([CH2:21][CH3:22])[CH2:19][CH3:20])[CH:7]=1)=[O:5])[CH3:2].[P:23](=[O:27])([OH:26])([OH:25])[OH:24]>>[P:23]([OH:27])([OH:26])([OH:25])=[O:24].[CH2:1]([O:3][C:4]([C:6]1[CH2:11][C@H:10]([NH2:12])[C@@H:9]([NH:13][C:14](=[O:16])[CH3:15])[C@H:8]([O:17][CH:18]([CH2:21][CH3:22])[CH2:19][CH3:20])[CH:7]=1)=[O:5])[CH3:2]参加物
3
実験手順
Form B may be formed by adding (3R,4R,5S)-4-acetylamino-5-amino-3-(1-ethyl-propoxy)-cyclohex-1-enecarboxylic acid ethyl ester to the phosphoric acid and cooling the supersaturated solution from 50° C. to −40° C. as fast as possible (without seeding).
後処理
- customForm B may be formed
- temperaturecooling the supersaturated solution from 50° C. to −40° C. as fast as possible (without seeding)
出典と根拠
- ORDレコード
- ord-0c10069f60fc4ba9a6e569cad3915ad6
- 出典データセット
- uspto-grants-2012_12
- 特許番号
- US08334319B2
関連ノート
読み込み中…