Réaction #438403

ord-c83a95c4f2d84e6ca5e1b908c3261342

Équation de réaction

Cl.NNc1ccc(OCc2ccccc2)cc1
1-[4-(benzyloxy)phenyl]hydrazine hydrochloride
Cl.NNc1ccc(OCc2ccccc2)cc1
1-[4-(Benzyloxy)phenyl]hydrazine hydrochloride
CC(C)(C)OC(=O)NCCOc1ccc(C(=O)CC(=O)C(F)(F)F)cc1
tert-butyl 2-[4-(4,4,4-trifluoro-3-oxobutanoyl)phenoxy]ethylcarbamate
CC(C)(C)OC(=O)NCCOc1ccc(C(=O)CC(=O)C(F)(F)F)cc1
tert-Butyl 2-[4-(4,4,4-trifluoro-3-oxobutanoyl)-phenoxy]ethylcarbamate
Cl.NCCOc1ccc(-c2cc(C(F)(F)F)nn2-c2ccc(OCc3ccccc3)cc2)cc1
title compound
Rendement 87.5%
Cl.NCCOc1ccc(-c2cc(C(F)(F)F)nn2-c2ccc(OCc3ccccc3)cc2)cc1
2-{4-[1-(4-Benzyloxyphenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl]phenoxyl}ethanamine hydrochloride
Rendement 87.5%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

The title compound (12.9 g, 87.5%) was prepared from 1-[4-(benzyloxy)phenyl]hydrazine hydrochloride obtained by Example 79-1 and tert-butyl 2-[4-(4,4,4-trifluoro-3-oxobutanoyl)phenoxy]ethylcarbamate obtained by Example 78-2 in a similar manner to that of Example 78-3.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07183306B2uspto-grants-2007_02