反应详情

A mixture of 10.0 g. (35 mmole) of 7-chloro-1,3-dihydro-1-methyl-5-phenyl-2H-1,4-benzodiazepin-2-one, 6.7 g. of aluminum chloride, 300 ml. of benzene and 30 ml. of hexane was chilled in an ice-bath and was treated with 10 ml. of propylene oxide. The reaction mixture was warmed to room temperature and was stirred overnight. Work-up as in Method A, Example 5, yielded a mixture of the epimers of 10-chloro-2,7-dimethyl-2,3,5,11b-tetrahydro-11b-phenyloxazole[3,2-d][1,4]benzodiazepin-6(7H)-one. A solution of 1.0 g. of this mixture was stirred overnight at 80° in 25 ml. of boron trifluoride etherate. The reaction mixture was poured carefully into ice water and made basic with ammonium hydroxide. The mixture was extracted with chloroform, water washed, dried and concentrated to a solid residue. Three recrystallizations from methylene chloride-hexane gave the above-titled isomer, m.. 142°-143°.

1. additionA mixture of 10.0 g
2. additionwas treated with 10 ml
3. customyielded
4. stirringof this mixture was stirred overnight at 80° in 25 ml
5. extractionThe mixture was extracted with chloroform, water
6. washwashed
7. customdried
8. concentrationconcentrated to a solid residue
9. customThree recrystallizations from methylene chloride-hexane
10. customgave the above-titled isomer, m
11. custom142°-143°