5-苄基-2-甲基-2,3-二氢-1H-1,5-苯并二氮杂-4-one

反应条件: temp:0.00; pressure:0.00; stir:

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: The titled compound was synthesized from 1-benzyl-4-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one and phthalimidoacetyl chloride in substantially the same manner as in Working Example 46. Yield 61%. m.p. 248°-250° C. (diethyl ether).

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: The titled compound was synthesized from 1-benzyl-4-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one and phthalimidoacetyl chloride in substantially the same manner as in Working Example 46. Yield 61%. m.p. 248°-250° C. (diethyl ether).

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: The titled compound was synthesized from 1-benzyl-4-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one and phthalimidoacetyl chloride in substantially the same manner as in Working Example 46. Yield 61%. m.p. 248°-250° C. (diethyl ether).

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: The titled compound was synthesized from 1-benzyl-4-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one and phthalimidoacetyl chloride in substantially the same manner as in Working Example 46. Yield 61%. m.p. 248°-250° C. (diethyl ether).