반응식
P([O-])(OCC)(SCC)=[S:2].[Cl:10][C:11]1[CH:12]=[C:13]([CH:35]=[CH:36][C:37]=1[O:38][CH3:39])[CH2:14][NH:15][C:16]1[C:25]2[C:20](=[CH:21][CH:22]=[C:23]([C:26]#[N:27])[CH:24]=2)[C:19]([N:28]2[CH2:33]CCC[CH:29]2O)=[N:18][N:17]=1.[CH:40]([OH:43])([CH3:42])[CH3:41]>O>[Cl:10][C:11]1[CH:12]=[C:13]([CH:35]=[CH:36][C:37]=1[O:38][CH3:39])[CH2:14][NH:15][C:16]1[C:25]2[C:20](=[CH:21][CH:22]=[C:23]([C:26](=[S:2])[NH2:27])[CH:24]=2)[C:19]([N:28]2[CH2:33][CH2:42][CH:40]([OH:43])[CH2:41][CH2:29]2)=[N:18][N:17]=1참가 물질
5
실험 절차
3.7 ml diethyl dithiophosphate was added to a mixture of 2.0 g 4-[(3-chloro-4-methoxybenzyl)amino]-1-(hydroxypiperidino)-6-phthalazine carbonitrile, 1 ml water and 2 ml isopropanol, and the mixture was heated under reflux for 1 hr. After cooling, water was added to the reaction solution and the resulting crystals were collected by filtration. The filtrate was extracted with ethyl acetate and washed with brine. It was dried over anhydrous sodium sulfate, and filtered. The filtrate was evaporated, and the resulting crystalline residue was combined with the crystals collected above by filtration, whereby 1.5 g of the title compound was obtained.
후처리
- temperaturethe mixture was heated
- temperatureunder reflux for 1 hr
- temperatureAfter cooling
- filtrationthe resulting crystals were collected by filtration
- extractionThe filtrate was extracted with ethyl acetate
- washwashed with brine
- dry with materialIt was dried over anhydrous sodium sulfate
- filtrationfiltered
- customThe filtrate was evaporated
- filtrationcollected above by filtration
출처 및 근거
- ORD 기록
- ord-5695479b783148a5bdc14f2c5cdf229d
- 출처 데이터셋
- uspto-grants-2004_03
- 특허 번호
- US06699870B2
연결된 노트
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