반응식
[Cl:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][C:5]([O:10][CH3:11])=[CH:4][C:3]=1[NH2:12].[CH2:13]([NH:15][C:16]1[C:21]([CH:22]=O)=[CH:20][N:19]=[C:18]([S:24][CH3:25])[N:17]=1)[CH3:14]>C1(C)C=CC=CC=1.S(=O)(=O)(O)O>[Cl:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][C:5]([O:10][CH3:11])=[CH:4][C:3]=1[N:12]=[CH:22][C:21]1[C:16]([NH:15][CH2:13][CH3:14])=[N:17][C:18]([S:24][CH3:25])=[N:19][CH:20]=1참가 물질
5
실험 절차
Into a solution of 3.78 g (20.2 mmol) of 2-chloro-3,5-dimethoxy-phenylamine in 110 mL of toluene was added 3.97 g (20.15 mmol) of 4-ethylamino-2-methylsulfanyl-pyrimidine-5-carbaldehyde. The reaction vessel was equipped with a Dean-Stark trap, and the reaction was warmed to reflux. After 3 hours, two drops of concentrated sulfuric acid were added to the reaction. The reaction was refluxed overnight then concentrated in vacuo to give 7.36 g (93%) of the title compound, which was used as is in the following example:
후처리
- customThe reaction vessel was equipped with a Dean-Stark trap
- temperaturethe reaction was warmed to reflux
- temperatureThe reaction was refluxed overnight
- concentrationthen concentrated in vacuo
출처 및 근거
- ORD 기록
- ord-5db665303cbf4edca956a9ab3e11c1fe
- 출처 데이터셋
- uspto-grants-2009_03
- 특허 번호
- US07501425B1
연결된 노트
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