반응식
[NH2:1][C:2]1[C:6]([NH2:7])=[C:5]([CH3:8])[S:4][C:3]=1[C:9]([O:11][CH3:12])=[O:10].Cl[C:14](Cl)([O:16]C(=O)OC(Cl)(Cl)Cl)Cl>CN(C)C=O.ClCCl>[CH3:8][C:5]1[S:4][C:3]([C:9]([O:11][CH3:12])=[O:10])=[C:2]2[C:6]=1[NH:7][C:14](=[O:16])[NH:1]2참가 물질
실험 절차
Methyl 3,4-diamino-5-methylthiophene-2-carboxylate (3.0 g) was dissolved in a mixture of N,N-dimethyl formamide (5 ml) and dichloromethane (15 ml). To the solution was added triphosgene (2.4 g) in portions. The mixture was stirred for two days at room temperature, and precipitates were collected by filtration, washed with dichloromethane and dried. Resultant white powder (2.4 g) was suspended in N,N-dimethylformamide (25 ml). To the suspension was added sodium hydride (60% in oil; 0.55 g), and the mixture was stirred for three days at room temperature. The solvent was evaporated under reduced pressure. To the residue was added 2N-HCl. Resulting precipitates were collected by filtration, washed with water, ether and methanol successively, followed by drying to afford the title compound (82 g, 53%) as pale brown powder.
후처리
- customprecipitates
- filtrationwere collected by filtration
- washwashed with dichloromethane
- customdried
- additionTo the suspension was added sodium hydride (60% in oil; 0.55 g)
- stirringthe mixture was stirred for three days at room temperature
- customThe solvent was evaporated under reduced pressure
- additionTo the residue was added 2N-HCl
- customResulting
- customprecipitates
- filtrationwere collected by filtration
- washwashed with water, ether and methanol successively
- customby drying
출처 및 근거
- ORD 기록
- ord-5a8b07a85d754ba09f86d8772e993268
- 출처 데이터셋
- uspto-grants-1993_09
- 특허 번호
- US05243054
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