反应 #1904061

ord-20fdc38743c14c0db2f0dbeb53948ac5

反应方程式

CC1(C)OCC(=O)Nc2ccc(Br)cc21
7-bromo-5,5-dimethyl-1,5-dihydro-4,1-benzoxazepin-2(3H)-one
CC(C)(C)OC(=O)n1cccc1B(O)O
2-borono-1H-pyrrole-1-carboxylic acid, 1-tert-butyl ester
CC(C)(C)OC(=O)n1cccc1-c1ccc2c(c1)C(C)(C)OCC(=O)N2
tert-Butyl 2-(5,5-dimethyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepin-7-yl)-1H-pyrrole-1-carboxylate

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

tert-Butyl 2-(5,5-dimethyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepin-7-yl)-1H-pyrrole-1-carboxylate was prepared from 7-bromo-5,5-dimethyl-1,5-dihydro-4,1-benzoxazepin-2(3H)-one and 2-borono-1H-pyrrole-1-carboxylic acid, 1-tert-butyl ester generally according to the procedure described in example 1. 1H-NMR (DMSO-d6) δ 9.96 (s, 1H), 7.32 (m, 1H), 7.23 (m, 1H), 7.15 (d, J=8.24 Hz, 1H), 7.07 (d, J=8.3 Hz, 1H), 6.25 (m, 2H), 4.23 (s, 2H), 1.55 (s, 6H), 1.36 (s, 9H); MS (ES) m/z 357 ([M+H]+, 100%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07598237B2uspto-grants-2009_10