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HRID 240594作成日:2026年10月25日

(S)-tert-butyl 3-(5-fluoro-2-nitrophenoxy)piperidine-1-carboxylate → (S)-tert-butyl 3-(2-amino-5-fluorophenoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/240594

反応式

関与物質

役割名称HCID仕込み量
反応物(S)-tert-butyl 3-(5-fluoro-2-nitrophenoxy)piperidine-1-carboxylateHCID 58413048—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物(S)-tert-butyl 3-(2-amino-5-fluorophenoxy)piperidine-1-carboxylateHCID 58413089—

反応手順

To a solution of (S)-tert-butyl 3-(5-fluoro-2-nitrophenoxy)piperidine-1-carboxylate (6.41 g) in MeOH (70.0 ml) was added palladium on charcoal (600.0 mg), the mixture hydrogenated at room temperature and 50 psi. The catalyst was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica chromatography to give the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08648068B2
出典データセットuspto-grants-2014_02
ORD IDord-88c079872f0242228e04ee046c9b1af7
出典メモuspto-grants-2014_02