反应详情

温度

40 °C

Dissolve 3-tert-butoxycarbonyl-7-chloro-6-dimethylcarbamoylthio-2,3,4,5-tetrahydro-1H-benzo[d]azepine (150 mg, 0.39 mmol) in methanol (10 mL) and add potassium hydroxide (0.7 g, 12.47 mmol). Heat at 60° C. for 4 h. Cool the reaction mixture to ambient temperature, add aqueous saturated ammonium chloride and concentrate in vacuo. Partition the residue between EtOAc and water. Dry the organic phase over anhydrous Na2SO4 and concentrate in vacuo to give 3-tert-butoxycarbonyl-7-chloro-6-mercapto-2,3,4,5-tetrahydro-1H-benzo[d]azepine (0.12 g). Dissolve the crude 3-tert-butoxycarbonyl-7-chloro-6-mercapto-2,3,4,5-tetrahydro-1H-benzo[d]azepine (0.12 g, 5.2 mmol) in anhydrous DMSO (6 mL) and add triethylamine (0.325 mL, 2.34 mmol) and 4-(pyridine-3-carbonyl)-benzyl methanesulfonate (114 mg, 0.39 mmol). Heat the solution at 40° C. overnight. Cool to ambient temperature, dilute the mixture with hexane/EtOAc (1:1, 100 mL), and wash the organic solution sequentially with brine and ice-cold water. Dry the organic layer over anhydrous Na2SO4, filter and concentrate in vacuo. Purify the crude mixture by chromatography on silica gel eluting with hexane and hexane/EtOAc (1:1) to give 3-tert-butoxycarbonyl-7-chloro-6-[4-(pyridine-3-carbonyl)-benzylthio]-2,3,4,5-tetrahydro-1H-benzo[d]azepine as oil (123 mg, 64%).

1. temperatureCool to ambient temperature
2. washwash the organic solution sequentially with brine and ice-cold water
3. dry with materialDry the organic layer over anhydrous Na2SO4
4. filtrationfilter
5. concentrationconcentrate in vacuo
6. customPurify the crude mixture by chromatography on silica gel eluting with hexane and hexane/EtOAc (1:1)