Reaction #1006009

ord-95e3a924d2b44626be2625145913e66b

Reaction equation

CC(C)(C)c1ccc(CN)cc1
(4-(tert-butyl)phenyl)methanamine
CCOC(=O)c1cn2cc(Br)ccc2n1
ethyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylate
CC(C)(C)c1ccc(CNC(=O)c2cn3cc(Br)ccc3n2)cc1
title compound
CC(C)(C)c1ccc(CNC(=O)c2cn3cc(Br)ccc3n2)cc1
6-Bromo-N-(4-(tert-butyl)benzyl)imidazo[1,2-a]pyridine-2-carboxamide

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Procedure

The title compound was prepared by essentially following the same procedures described for Intermediate I, using (4-(tert-butyl)phenyl)methanamine and ethyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylate as starting materials. 1H NMR (400 MHz, CDCl3) δ 9.53 (s, 1H), 8.60 (s, 1H), 8.41 (s, 1H), 7.88 (d, 1H), 7.79 (d, 1H), 7.36 (d, 2H), 7.32 (d, 2H), 4.60 (d, 2H), 1.38 (s, 9H). MS 385.9, 387.9 (M+1)+.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09271969B2uspto-grants-2016_03