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HRID 15021作成日:2026年10月26日

1,1-Dimethylethyl (trans)-3-hydroxy4-[[(phenylmethyl)amino]methyl]-1-piperidinecarboxylate → trans-1-Boc-4-aminomethyl-3-hydroxypiperidine

https://huagongshe.com/reaction/15021

反応式

関与物質

役割名称HCID仕込み量
反応物1,1-Dimethylethyl (trans)-3-hydroxy4-[[(phenylmethyl)amino]methyl]-1-piperidinecarboxylateHCID 11738727—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物trans-1-Boc-4-aminomethyl-3-hydroxypiperidineHCID 11075229—

反応手順

A mixture of 1,1-dimethylethyl(trans)-3-hydroxy-4-[[(phenylmethyl)amino]methyl]-1-piperidinecarboxylate [described in WO-00/37461 as intermediate (1-d)] (0.023 mol) in methanol (100 ml) was hydrogenated with palladium-on-carbon (10%, 1 g) as a catalyst. After uptake of hydrogen (1 equivalent), the catalyst was filtered off and the filtrate was evaporated. The residue was solidified in DIPE+ACN, filtered off and dried, yielding 4 g of 1,1-dimethylethyl(trans)-4-(aminomethyl)-3-hydroxy-1-piperidinecarboxylate (intermediate 42, mp. 178° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732464B2
出典データセットuspto-grants-2010_06
ORD IDord-08c72e7bee6743eea190c6b28c14c77b
出典メモuspto-grants-2010_06