反应 #586169

ord-8eeb5fd0bebb403193bc6b4eb854ffd4

反应方程式

O=S(=O)(O)O
sulfuric acid
Cl.NNc1ccc(Br)cc1
4-bromophenylhydrazine hydrochloride
CC(=O)[O-].[Na+]
sodium acetate
O=C1CCC(=O)c2ccccc2N1
1H-[1]benzazepin-2,5(3H, 4H)-dione
CC(=O)[O-].[Na+]
sodium acetate
O=C1Cc2c([nH]c3ccc(Br)cc23)-c2ccccc2N1
title compound
收率 86.3%
O=C1Cc2c([nH]c3ccc(Br)cc23)-c2ccccc2N1
9-Bromo-7,12-dihydroindolo[3,2-d][1]-benzazepin-6(5H)-one
收率 86.3%

反应条件

温度
70°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度cooled
  2. 2
    温度before heating at 70° C. for a further 3 hours
  3. 3
    过滤the precipitate filtered

实验过程

To a suspension of 1H-[1]benzazepin-2,5(3H, 4H)-dione (0.247 g, 1.3 mmol) in acetic acid (5 ml) was added 4-bromophenylhydrazine hydrochloride (0.532 g, 2.3 mmol) and sodium acetate (0.195 g, 2.3 mmol) and stirred under argon. The mixture was heated at 70° C. for 3 hours, then cooled and concentrated sulfuric acid (0.5 ml) added, before heating at 70° C. for a further 3 hours. The slurry was poured into 10% sodium acetate aqueous solution (20 ml) and the precipitate filtered to give the title compound as a cream solid (0.367 g, yield 79.6%), mp>300° C.; 1H-NMR (DMSO-d6, 300 MHz): δ (ppm)=11.82 (s; 1 H), 10.1 (s; 1H), 7.89 (d; 1H), 7.74 (dd; 1H), 7.41-7.36 (m; 2H), 7.30-7.21 (m; 3H), 3.51 (s; 2H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07767664B2uspto-grants-2010_08