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HRID 335016作成日:2026年10月24日

Diethyl Ether → (S)-2-(4-nitrophenyl)-1-(thiophen-2-ylthiazol-4-yl)ethanamine hydrobromide salt

https://huagongshe.com/ja/reaction/335016

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物2-ThiophenecarbothioamideHCID 737237—
反応物(S)-tert-Butyl (4-bromo-1-(4-nitrophenyl)-3-oxobutan-2-yl)carbamateHCID 53778469—
溶媒AcetonitrileHCID 6342—
生成物(S)-2-(4-nitrophenyl)-1-(thiophen-2-ylthiazol-4-yl)ethanamine hydrobromide saltHCID 6670471887%

反応手順

A mixture of (S)-tert-butyl 4-bromo-1-(4-nitrophenyl)-3-oxobutan-2-ylcarbamate, 7, (7.74 g, 20 mmol), and thiophen-2-carbothioic acid amide (3.14 g, 22 mmol) in CH3CN (200 mL) is refluxed for 5 hours. The reaction mixture is cooled to room temperature and diethyl ether (50 mL) is added to the solution. The precipitate which forms is collected by filtration. The solid is dried under vacuum to afford 7.14 g (87% yield) of the desired product. ESI+ MS 332 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08883832B2
出典データセットuspto-grants-2014_11
ORD IDord-5067efa4c7a84917975dbe308d67e92b
出典メモuspto-grants-2014_11