反应 #1797512

ord-2643842220ca488f9925f651633bb507

反应方程式

COc1ccc(Cl)cc1B(O)O
2-methoxy-5-chlorophenylboronic acid
O=C(O)c1ccc(B(O)O)cc1
4-carboxyphenylboronic acid
Brc1cccc(-c2nnn[nH]2)c1
5-(3-bromophenyl)-1H-tetrazole
COc1ccc(Cl)cc1-c1cccc(-c2nnn[nH]2)c1
title compound
COc1ccc(Cl)cc1-c1cccc(-c2nnn[nH]2)c1
5-(5′-chloro-2′-methoxybiphenyl-3-yl)-1H-tetrazole

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Following the procedure of Example 1b), except substituting 2-methoxy-5-chlorophenylboronic acid; for 4-carboxyphenylboronic acid; and substituting 5-(3-bromophenyl)-1H-tetrazole for the compound of 1a), the title compound was prepared (1.36 g; 100%) as a white solid. 1H NMR (300 MHz, d6-DMSO) δ 8.16 (s, 1H), 8.05 (d, J=7.6 Hz, 1H), 7.7 (d, J=6.6 Hz, 1H), 7.67 (t, J=7.7 Hz, 1H), 7.48 (m, 2H), 7.2 (d, J=9.1 Hz, 1H), 3.8 (s, 3H), MS (ES) m/z 287 [M+H].

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07790704B2uspto-grants-2010_09