反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[CH2:14][CH:13]([CH2:15][CH:16]3[CH2:21][CH2:20][N:19]([CH2:22][C:23]4[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=4)[CH2:18][CH2:17]3)[C:11](=[O:12])[C:6]2=[CH:7][C:8]=1[O:9][CH3:10].[ClH:29]>C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[CH2:14][CH:13]([CH2:15][CH:16]3[CH2:17][CH2:18][N:19]([CH2:22][C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)[CH2:20][CH2:21]3)[C:11](=[O:12])[C:6]2=[CH:7][C:8]=1[O:9][CH3:10].[ClH:29]参加物
4
反応条件
- 温度
- 9 °C
実験手順
50 g of donepezil was dissolved by stirring in 240 g of ethanol under heating, followed by adding 15.1 g of concentrated hydrochloric acid thereto at the internal temperature of 30° C. Then, it was cooled and continued stirring while keeping the internal temperature at about 25° C. Crystals started precipitating about 1 hour after the concentrated hydrochloric acid was poured into the mixture. After the precipitation started, the mixture was stirred at the internal temperature of 25° C. for 17 hours and then cooled to the internal temperature of 9° C. The crystals were collected by filtration and dried about 3 hours after the cooling was started, to give 52.25 g of polymorphic crystal (III) of donepezil hydrochloride (yield: 95.3%).
後処理
- temperatureunder heating
- customat the internal temperature of 30° C
- temperatureThen, it was cooled
- customat about 25° C
- customCrystals started precipitating about 1 hour after the concentrated hydrochloric acid
- additionwas poured into the mixture
- customAfter the precipitation
- stirringthe mixture was stirred at the internal temperature of 25° C. for 17 hours
- filtrationThe crystals were collected by filtration
- customdried about 3 hours after the cooling
出典と根拠
- ORDレコード
- ord-03340c938c664c9abbd4b96929af37bd
- 出典データセット
- uspto-grants-2009_01
- 特許番号
- US07479563B2
関連ノート
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