반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:14]([NH2:15])=[N:13][C:12]([N:16]3[CH2:21][CH2:20][N:19]([C:22]([CH:24]4[O:33][C:32]5[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=5[O:26][CH2:25]4)=[O:23])[CH2:18][CH2:17]3)=[N:11][C:6]2=[CH:7][C:8]=1[O:9][CH3:10].[CH3:34][S:35]([OH:38])(=[O:37])=[O:36]>CC(C)=O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:14]([NH2:15])=[N:13][C:12]([N:16]3[CH2:17][CH2:18][N:19]([C:22]([CH:24]4[O:33][C:32]5[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=5[O:26][CH2:25]4)=[O:23])[CH2:20][CH2:21]3)=[N:11][C:6]2=[CH:7][C:8]=1[O:9][CH3:10].[CH3:34][S:35]([OH:38])(=[O:37])=[O:36]참가 물질
4
반응 조건
- 온도
- 25 °C
실험 절차
Doxazosin base (0.277 mol; 125 g) was charged in acetone (1875 ml) and stirred at 25° C. to obtain slurry. On cooling the slurry to 10-15° C., methanesulphonic acid (0.33 mol; 31.96 g) was added to it. The contents were stirred for 10-15 min at 10-15° C. and then stirring continued at 25° C. for 2 hr. The solid obtained was filtered, washed with acetone and dried at 50-55° C. to obtain solid. The solid was purified by refluxing in methanol (1500 ml) for 1 hr. The slurry was cooled to room temperature, filtered, washed with methanol and then dried at 60° C. under reduced pressure to obtain 135 g of pure doxazosin mesylate (HPLC purity −99.81%).
후처리
- customto obtain slurry
- temperatureOn cooling the slurry to 10-15° C.
- stirringThe contents were stirred for 10-15 min at 10-15° C.
- stirringstirring
- customThe solid obtained
- filtrationwas filtered
- washwashed with acetone
- customdried at 50-55° C.
- customto obtain solid
- customThe solid was purified
- temperatureby refluxing in methanol (1500 ml) for 1 hr
- temperatureThe slurry was cooled to room temperature
- filtrationfiltered
- washwashed with methanol
- customdried at 60° C. under reduced pressure
출처 및 근거
- ORD 기록
- ord-9ce08473a972475283b8c15229ce2a66
- 출처 데이터셋
- uspto-grants-2013_04
- 특허 번호
- US08426590B2
연결된 노트
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