反応式
[CH3:1][C@@H:2]([NH:13][CH2:14][CH2:15][CH2:16][C:17]1[CH:18]=[CH:19][CH:20]=[C:21]([C:23]([F:26])([F:25])[F:24])[CH:22]=1)[C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=12.[ClH:27]>C(OCC(C)C)(=O)C>[CH3:1][C@@H:2]([NH:13][CH2:14][CH2:15][CH2:16][C:17]1[CH:18]=[CH:19][CH:20]=[C:21]([C:23]([F:24])([F:25])[F:26])[CH:22]=1)[C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=12.[ClH:27]参加物
4
実験手順
0.3 g of cinacalcet base was dissolved in 4 ml of isobutyl acetate at room temperature, i.e., about 20° to about 25° C. Then, 2 ml of 1N HCl were added in one portion, and the mixture was stirred at room temperature overnight, yielding a precipitate. The product was isolated by filtration, washed with 5 ml of isobutyl acetate, and dried at 50° C. in a vacuum oven for 24 hours, yielding 0.12 g of cinacalcet hydrochloride crystalline Form I.
後処理
- customi.e., about 20° to about 25° C
- customyielding a precipitate
- customThe product was isolated by filtration
- washwashed with 5 ml of isobutyl acetate
- customdried at 50° C. in a vacuum oven for 24 hours
出典と根拠
- ORDレコード
- ord-91fddeac19ad41778c823f1730f626b8
- 出典データセット
- uspto-grants-2007_07
- 特許番号
- US07247751B2
関連ノート
読み込み中…