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HRID 42165作成日:2026年10月25日

5-Isopropenyl-2-[4-[2-(4-methanesulfonylphenoxymethyl)pyridin-5-yl]piperidin-1-yl]pyrimidine → 5-Isopropyl-2-[4-[2-(4-methanesulfonylphenoxymethyl)pyridin-5-yl]piperidin-1-yl]pyrimidine

https://huagongshe.com/reaction/42165

反応式

関与物質

役割名称HCID仕込み量
反応物5-Isopropenyl-2-[4-[2-(4-methanesulfonylphenoxymethyl)pyridin-5-yl]piperidin-1-yl]pyrimidineHCID 67083237—
触媒HCID 178418390HCID 178418390—
溶媒MethanolHCID 887—
生成物5-Isopropyl-2-[4-[2-(4-methanesulfonylphenoxymethyl)pyridin-5-yl]piperidin-1-yl]pyrimidineHCID 6708302971.4%

反応手順

To a solution of 5-isopropenyl-2-[4-[2-(4-methanesulfonylphenoxymethyl)pyridin-5-yl]piperidin-1-yl]pyrimidine (Example 58) (21 mg, 0.045 mmol) in methanol (0.45 mL) was added 10% palladium-carbon (10 mg). The mixture was hydrogenated at room temperature for 1 hour and filtered through Celite pad. The filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/2) to give the title compound as a white crystal (15 mg, yield 71%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536176B2
出典データセットuspto-grants-2013_09
ORD IDord-3559dbb87a5e42068d107d1e4d553271
出典メモuspto-grants-2013_09