Реакция #57205

ord-8b049bdae8d5458bba981971cd72863f

Уравнение реакции

O=[N+]([O-])c1ccc(-c2n[nH]cc2Br)cc1
4-bromo-3-(4-nitrophenyl)-1H-pyrazole
COc1ccc(CCl)cc1
p-methoxybenzylchloride
→
COc1ccc(Cn2cc(Br)c(-c3ccc([N+](=O)[O-])cc3)n2)cc1
title product
COc1ccc(Cn2cc(Br)c(-c3ccc([N+](=O)[O-])cc3)n2)cc1
4-bromo-1-{[4-(methyloxy)phenyl]methyl}-3-(4-nitrophenyl)-1H-pyrazole

Реактанты

—
Intermediate 3
O=[N+]([O-])c1ccc(-c2n[nH]cc2Br)cc1
4-bromo-3-(4-nitrophenyl)-1H-pyrazole
COc1ccc(CCl)cc1
p-methoxybenzylchloride

Реагенты

Нет

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

Following the procedure described for Intermediate 3 with 4-bromo-3-(4-nitrophenyl)-1H-pyrazole and p-methoxybenzylchloride provided the title product. ESMS [M+H]+: 388.2

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07419988B2uspto-grants-2008_09