Reacción #43185

ord-4b4178151fca419dac819ae8ff154559

Ecuación de reacción

O=Cc1cccc(-c2ccnc(Cl)n2)c1
3-(2-Chloro-pyrimidin-4-yl)-benzaldehyde
O=Cc1cccc(-c2ccnc(Cl)n2)c1
intermediate 1
O=Cc1cccc(-c2ccnc(Cl)n2)c1
3-(2-Chloro-pyrimidin-4-yl)-benzaldehyde
CC(C)(C)N
tert butylamine
CC(C)(C)NCc1cccc(-c2ccnc(Cl)n2)c1
tert-Butyl-[3-(2-chloro-pyrimidin-4-yl)-benzyl]-amine
Rendimiento 97.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

3-(2-Chloro-pyrimidin-4-yl)-benzaldehyde (intermediate 1) and tert butylamine were coupled by procedure B. The yield was 97%. LC-MS showed the product had the expected M+H+ of 276. 1H NMR (Varian 300 MHz, CDCl3, shifts relative to the solvent peak at 7.24 ppm) 8.6 (d, 1H) 8.1 (s, 1H) 7.9 (d, 1H) 7.6 (d, 1H) 7.5 (m, 2H) 1.2 (s, 9H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07732444B2uspto-grants-2010_06