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HRID 417168作成日:2026年10月26日

4-{(E)-3-cyclohexyl-3-[2-(2,6-dimethoxy-pyridin-3-yl)-5,6-difluoro-benzoimidazol-1-yl]-propenyl}-benzoic acid methyl ester → 4-{3-Cyclohexyl-3-[2-(2,6-dimethoxy-pyridin-3-yl)-5,6-difluoro-benzoimidazol-1-yl]-propyl}-benzoic acid methyl ester

https://huagongshe.com/reaction/417168

反応式

関与物質

役割名称HCID仕込み量
反応物4-{(E)-3-cyclohexyl-3-[2-(2,6-dimethoxy-pyridin-3-yl)-5,6-difluoro-benzoimidazol-1-yl]-propenyl}-benzoic acid methyl esterHCID 66619459—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物4-{3-Cyclohexyl-3-[2-(2,6-dimethoxy-pyridin-3-yl)-5,6-difluoro-benzoimidazol-1-yl]-propyl}-benzoic acid methyl esterHCID 66619495—

反応手順

To a solution of 210 mg (0.383 mmol) 4-{(E)-3-cyclohexyl-3-[2-(2,6-dimethoxy-pyridin-3-yl)-5,6-difluoro-benzoimidazol-1-yl]-propenyl}-benzoic acid methyl ester in 4 ml methanol was added 30 mg Pd on carbon 5%. The reaction mixture was hydrogenated at 1.5 bar under vigorous stirring for 1 hour, then filtered over dicalite and concentrated under vacuum. Colorless oil (90%). MS (Turbo Spray): m/z=550.4 [M+H].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08088930B2
出典データセットuspto-grants-2012_01
ORD IDord-1d18229c3bc94faf882c5ca21b644fc6
出典メモuspto-grants-2012_01