Reacción #487973

ord-6aaf966657d74fae9665bb181a26cdbb

Ecuación de reacción

CC(C)(C)c1nc(Cl)c2nnn(Cc3ccccc3Cl)c2n1
5-tert-butyl-7-chloro-3-(2-chlorobenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine
Cl.FC1(F)CCNCC1
4,4-difluoropiperidine hydrochloride
CC(C)(C)c1nc(N2CCOCC2)c2nnn(Cc3ccccc3Cl)c2n1
5-tert-butyl-3-(2-chloro-benzyl)-7-morpholin-4-yl-3H-[1,2,3]triazolo[4,5-d]pyrimidine
CC(C)(C)c1nc(N2CCOCC2)c2nnn(Cc3ccccc3Cl)c2n1
5-tert-Butyl-3-(2-chloro-benzyl)-7-morpholin-4-yl-3H-[1,2,3]triazolo[4,5-d]pyrimidine
CC(C)(C)c1nc(N2CCC(F)(F)CC2)c2nnn(Cc3ccccc3Cl)c2n1
title compound
CC(C)(C)c1nc(N2CCC(F)(F)CC2)c2nnn(Cc3ccccc3Cl)c2n1
5-tert-Butyl-3-(2-chloro-benzyl)-7-(4,4-difluoro-piperidin-1-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

In analogy to the procedure described for the synthesis of 5-tert-butyl-3-(2-chloro-benzyl)-7-morpholin-4-yl-3H-[1,2,3]triazolo[4,5-d]pyrimidine (example 1, step c), the title compound was prepared from 5-tert-butyl-7-chloro-3-(2-chlorobenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine and 4,4-difluoropiperidine hydrochloride and isolated as light-yellow gum (10.9 mg, 55%). MS (m/e): 421.4 (MH+).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08741906B2uspto-grants-2014_06