Реакция #645779

Уравнение реакции

6-(4-chloro-phenyl)-3-iodo-8-methyl-imidazo[1,2-a]pyridine

6-(4-Chloro-phenyl)-3-iodo-8-methyl-imidazo[1,2-a]pyridine

trimethylsilylacetylene

→

title compound

Выход 80.0%

6-(4-Chloro-phenyl)-8-methyl-3-trimethylsilanylethynyl-imidazo[1,2-a]pyridine

Выход 80.0%

Условия реакции

Методика

Prepared from 6-(4-chloro-phenyl)-3-iodo-8-methyl-imidazo[1,2-a]pyridine (example C.21 step 2) (3.686 g, 10 mmol) and trimethylsilylacetylene (2.8 mL, 20 mmol) as described in example C.20 step 4. Obtained the title compound as a yellow foam (2.70 g, 80%). MS (ISP) 339.1 [(M+H)+], 341 [(M+2+H)+].

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