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HRID 42139作成日:2026年10月27日

Tert-Butyl 4-[2-(4-methanesulfonylbenzoylamino)-pyridin-5-yl]-3,6-dihydro-2H-pyridine-1-carboxylate → Tert-Butyl 4-[2-(4-methanesulfonylbenzoylamino)pyridin-5-yl]piperidine-1-carboxylate

https://huagongshe.com/reaction/42139

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-Butyl 4-[2-(4-methanesulfonylbenzoylamino)-pyridin-5-yl]-3,6-dihydro-2H-pyridine-1-carboxylateHCID 67083258—
触媒HCID 178418390HCID 178418390—
溶媒MethanolHCID 887—
生成物Tert-Butyl 4-[2-(4-methanesulfonylbenzoylamino)pyridin-5-yl]piperidine-1-carboxylateHCID 6708325257%

反応手順

To a solution of tert-butyl 4-[2-(4-methanesulfonylbenzoylamino)pyridin-5-yl]-3,6-dihydro-2H-pyridine-1-carboxylate (83 mg, 0.18 mmol) in methanol (2 mL) was added 10% palladium-carbon (8.3 mg). The mixture was hydrogenated at room temperature for 4 hours and filtered through Celite pad. The filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=2/3) to give the title compound as a white crystal (47 mg, yield 57%).

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-0d304eb99e614532af5208d05dd039ab
出典メモuspto-grants-2013_09