1,1'-Thiocarbonyldi-2(1H)-pyridone → 4-Methoxycarbonyl-3-nitrophenyl isothiocyanate
반응식
[NH2:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[C:4]([N+:12]([O-:14])=[O:13])[CH:3]=1.[C:15](N1C=CC=CC1=O)(N1C=CC=CC1=O)=[S:16]>ClCCl>[CH3:9][O:8][C:6]([C:5]1[CH:10]=[CH:11][C:2]([N:1]=[C:15]=[S:16])=[CH:3][C:4]=1[N+:12]([O-:14])=[O:13])=[O:7]참가 물질
4
실험 절차
A solution of the above synthesized methyl 4-amino-2-nitrobenzoate (50 mg, 0.25 mmol) and 1,1′-thiocarbonyldi-2(1H)-pyridone (59 mg, 0.25 mmol) in dichloromethane (4.2 ml) was stirred at room temperature for 3 hours. After completion of the reaction, the solvent was evaporated, followed by purification with a silica gel column chromatography to obtain 42 mg of the desired product as a colorless oil (yield 69%).
후처리
- customAfter completion of the reaction
- customthe solvent was evaporated
- customfollowed by purification with a silica gel column chromatography
출처 및 근거
- ORD 기록
- ord-7736916130734166a97567cd54cd8f85
- 출처 데이터셋
- uspto-grants-2009_08
- 특허 번호
- US07576115B2
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