反应 #955929

ord-cae0e8e657de4f19a5a33b3e5bff61b1

反应方程式

BrCc1ccccc1
benzyl bromide
Cc1ccc(-c2ccc(=S)[nH]n2)c(C)c1
6-(2,4-dimethylphenyl)pyridazine-3(2H)-thione
Cc1ccc(-c2ccc(=S)[nH]n2)c(C)c1
6-(2,4-Dimethylphenyl)pyridazine-3(2H)-thione
Cc1ccc(-c2ccc(SCc3ccccc3)nn2)c(C)c1
3-(Benzylthio)-6-(2,4-dimethylphenyl)pyridazine

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Prepared in a similar manner to example 13 using benzyl bromide and 6-(2,4-dimethylphenyl)pyridazine-3(2H)-thione (Example 13a). Yield 53.5 mg (38%). 1H NMR (300 MHz, dMSO): δ 2.29 (s, 3H), 2.34 (s, 3H), 4.60 (s, 2H), 7.16-7.17 (m, 2H), 7.30-7.34 (m, 4H), 7.47-7.49 (d, 2H), 7.64-7.72 (m, 2H); MS (M+H, 307).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08968708B2uspto-grants-2015_03