Реакция #2325317

ord-b4625b5024154ca4ad7ec2cbf0481d37

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

The title compound was prepared from 6-(4-chloro-phenyl)-3-iodo-8-methyl-imidazo[1,2-a]pyridine (example C.21 step 2) (737 mg, 2 mmol) and 5-ethynyl-pyridin-2-ylamine (example D.1) (307 mg, 2.6 mmol) according to general procedure II. Obtained as an off-white solid (240 mg, 33%). MS (ISP) 359.0 [(M+H)+], 361.0 [(M+2+H)+]; mp 231-234° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07718661B2uspto-grants-2010_05