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HRID 221375作成日:2026年10月26日

4-(Bromoacetyl)pyridine hydrobromide → 4-(4-Pyridin-4-yl-thiazol-2-ylmethoxy)piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/221375

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Bromoacetyl)pyridine hydrobromideHCID 2776239—
反応物Tert-butyl 4-(carbamothioylmethoxy)piperidine-1-carboxylateHCID 45496681—
溶媒MethanolHCID 887—
溶媒Ethyl AcetateHCID 8857—
生成物4-(4-Pyridin-4-yl-thiazol-2-ylmethoxy)piperidine-1-carboxylic acid tert-butyl esterHCID 57954451—

反応手順

A solution of 2-bromo-1-pyridin-4-yl-ethanone hydrobromide (35 mg, 1241 mol) and 4-thiocarbamoylmethoxypiperidine-1-carboxylic acid tert-butyl ester (Preparation 18, 34 mg, 124 μmol) in methanol (2 ml) was heated at 60° C. for 1.5 h. The reaction mixture was diluted with EtOAc (60 ml), washed with saturated aqueous NaHCO3 (15 ml) and brine (15 ml) then dried (MgSO4). The solvent was removed and the residue purified by flash chromatography (EtOAc) to afford the title compound: RT=2.95 ml, m/z (ES+)=376.1 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207147B2
出典データセットuspto-grants-2012_06
ORD IDord-af4f12460c324f09932ce5267922013d
出典メモuspto-grants-2012_06