반응식
[CH3:1][C:2]([C:5]#[C:6]/[CH:7]=[CH:8]/[CH2:9][N:10]([CH2:12][C:13]1[CH:14]=[CH:15][CH:16]=[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=12)[CH3:11])([CH3:4])[CH3:3].[ClH:23]>CC(C)=O>[CH3:4][C:2]([C:5]#[C:6]/[CH:7]=[CH:8]/[CH2:9][N:10]([CH2:12][C:13]1[CH:14]=[CH:15][CH:16]=[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=12)[CH3:11])([CH3:1])[CH3:3].[ClH:23]참가 물질
4
반응 조건
- 온도
- 20 °C
실험 절차
19.2 g crude terbinafine base (57.2 mmol theoretical, example 6) is dissolved in 83 ml acetone and then 6.2 ml (0.0631 mol) of 32% aqueous hydrochloric acid is added dropwise. The resulting suspension is stirred for 30 minutes at 20° C. and then cooled to −5°/−10° C. and stirred for a further 2.5 hours. The precipitate is filtered, washed with 16 ml cold acetone and dried to constant weight at 40° C. in a vacuum oven. 10.8 g (57.5% yield) terbinafine-HCl is obtained as a white solid with purity in excess of 99.8% (HPLC A %).
후처리
- temperaturecooled to −5°/−10° C.
- stirringstirred for a further 2.5 hours
- filtrationThe precipitate is filtered
- washwashed with 16 ml cold acetone
- customdried to constant weight at 40° C. in a vacuum oven
출처 및 근거
- ORD 기록
- ord-9656c80af1014b1db5c11620bc6d11f4
- 출처 데이터셋
- uspto-grants-2010_11
- 특허 번호
- US07838704B2
연결된 노트
불러오는 중…