Реакция #1875615

Уравнение реакции

Compound 204

2-{2-[4′-Chloro-4-(pyrrolidine-1-carbonyl)-biphen-2-yl]-quinolin-6-yl}-1-cyclohexyl-1H-benzoimidazole-5-carboxylic acid

Compound 25

3-({2-[4′-Chloro-4-(pyrrolidine-1-carbonyl)-biphen-2-yl]-quinoline-6-carbonyl}-amino)-4-cyclohexylamino-benzoic acid ethyl ester

acetophenone

→

title compound

1-Cyclohexyl-2-{2-[3-(pyrrolidine-1-carbonyl)-phenyl]-quinolin-6-yl}-1H-benzoimidazole-5-carboxylic acid

Условия реакции

Методика

The title compound was synthesized in four steps as described for Compound 13, Compound 25, Compound 27 Q=ethyl and Compound 204, respectively, except the product of the previous step was used in the first step, instead of acetophenone.

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