Pyridine → 7-bromo-2,3-dihydro-5-(2-pyridyl)-2-thioxo-1H-1,4-benzodiazepin-1-acetic acid methyl ester
반응식
[CH3:1][O:2][C:3](=[O:24])[CH2:4][N:5]1[C:11]2[CH:12]=[CH:13][C:14]([Br:16])=[CH:15][C:10]=2[C:9]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][N:18]=2)=[N:8][CH2:7][C:6]1=O.P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:26].N1C=CC=CC=1>C(Cl)Cl.O>[CH3:1][O:2][C:3](=[O:24])[CH2:4][N:5]1[C:11]2[CH:12]=[CH:13][C:14]([Br:16])=[CH:15][C:10]=2[C:9]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][N:18]=2)=[N:8][CH2:7][C:6]1=[S:26]참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
A mixture of 0.01 mole of 7-bromo-2,3-dihydro-5-(2-pyridyl)-2-oxo-1H-1,4-benzodiazepin-1-acetic acid methyl ester, 0.0105 mole of phosphorus pentasulfide and 100 ml. of pyridine is heated under reflux for about 24 hours. The mixture is evaporated and the residue thus obtained is dissolved in methylene chloride-water. The organic layer is separated, washed with saturated sodium bicarbonate solution, dried over anhydrous magnesium sulfate and evaporated to remove the solvent. The residue thus obtained is chromatographed on silica gel and eluted to give 7-bromo-2,3-dihydro-5-(2-pyridyl)-2-thioxo-1H-1,4-benzodiazepin-1-acetic acid methyl ester.
후처리
- temperatureunder reflux for about 24 hours
- customThe mixture is evaporated
- customthe residue thus obtained
- customThe organic layer is separated
- washwashed with saturated sodium bicarbonate solution
- dry with materialdried over anhydrous magnesium sulfate
- customevaporated
- customto remove the solvent
- customThe residue thus obtained
- customis chromatographed on silica gel
- washeluted
출처 및 근거
- ORD 기록
- ord-5011f439f2ee4783a9689880890692e2
- 출처 데이터셋
- uspto-grants-1976_01
- 특허 번호
- US03933816
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