1-[(4-乙氧基苯基)甲基]环丙-1-胺

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

实验步骤: Prepared according to general method 3 from 329 mg (1 mmol) 5-benzyloxy-8-(2,2-dihydroxy-acetyl)-4H-benzo[1,4]oxazin-3-one and 191 mg (1 mmol) 1-(4-ethoxy-benzyl)-cyclopropylamine. Yield: 17 mg (3%, trifluoroacetate); mass spectroscopy: [M+H]+=399. Prepared

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

实验步骤: Prepared according to general method 3 from 329 mg (1 mmol) 5-benzyloxy-8-(2,2-dihydroxy-acetyl)-4H-benzo[1,4]oxazin-3-one and 191 mg (1 mmol) 1-(4-ethoxy-benzyl)-cyclopropylamine. Yield: 17 mg (3%, trifluoroacetate); mass spectroscopy: [M+H]+=399. Prepared

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

实验步骤: Prepared according to general method 3 from 329 mg (1 mmol) 5-benzyloxy-8-(2,2-dihydroxy-acetyl)-4H-benzo[1,4]oxazin-3-one and 191 mg (1 mmol) 1-(4-ethoxy-benzyl)-cyclopropylamine. Yield: 17 mg (3%, trifluoroacetate); mass spectroscopy: [M+H]+=399. Prepared