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HRID 1160345作成日:2026年10月26日

Pyridine → N-BOC-3(R)-methylsulfonyloxymethyl-piperidine

https://huagongshe.com/reaction/1160345

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Methanesulfonyl chlorideHCID 31297—
反応物tert-Butyl 3-(hydroxymethyl)piperidine-1-carboxylateHCID 2763851—
溶媒DichloromethaneHCID 6344—
生成物N-BOC-3(R)-methylsulfonyloxymethyl-piperidineHCID 10108453—

反応手順

To a stirred solution of N—BOC-3-piperidinemethanol (0.50 g, 0.002 mmole) in DCM (10 mL) was added dropwise pyridine (2.42 mL, 0.03 mmole) followed by the addition of methanesulfonyl chloride (0.774 mL, 0.01 mmole). The reaction mixture continued stirring at RT overnight. The reaction mixture was quenched with water. The aqueous layer was extracted with EtOAc (3×5 mL). Combined organic layers were dried over Na2SO4 and concentrated to yield a crude oil, 68, which was used in the next step without further purification. LRMS: 193 (M+-BOC group).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07816375B2
出典データセットuspto-grants-2010_10
ORD IDord-a94c232791c6417ca5b9f80a4945474c
出典メモuspto-grants-2010_10