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HRID 41673作成日:2026年10月24日

Triglyme → 5-{1-[2-(4-Bromo-2-methyl-phenyl)-thiazol-5-yl]-ethoxy}-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one

https://huagongshe.com/ja/reaction/41673

反応式

関与物質

役割名称HCID仕込み量
反応物TriglymeHCID 8189—
反応物Sodium hydrideHCID 24758—
反応物1-[2-(4-Bromo-2-methyl-phenyl)-thiazol-5-yl]-ethanolHCID 59584676—
反応物5-Chloro-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-oneHCID 68567844—
溶媒TetrahydrofuranHCID 8028—
生成物5-{1-[2-(4-Bromo-2-methyl-phenyl)-thiazol-5-yl]-ethoxy}-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-oneHCID 6877358573.2%

反応手順

To a solution of [2-(4-bromo-2-methyl-phenyl)-thiazol-5-yl]-ethanol (450 mg, 1.5 mmol) and 5-chloro-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one (277 mg, 1.5 mmol) in tetrahydrofuran (10 ml) is added in one portion the sodium hydride (60% dispersion in mineral oil, 60 mg, 1.5 mmol). The reaction mixture is stirred at room temperature for 24 hours. The crude reaction mixture is vacced down under reduced pressure and 10 ml of triglyme are added. The reaction mixture is therefore heated to reflux for 30 minutes. The crude reaction mixture is vacced down and purified by flash chromatography on silica gel to give a yellow solid. The solid is washed with iso-hexane to give 5-{1-[2-(4-bromo-2-methyl-phenyl)-thiazol-5-yl]-ethoxy}-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one (490 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530667B2
出典データセットuspto-grants-2013_09
ORD IDord-d1656d9515194173a1d6413fd2f90966
出典メモuspto-grants-2013_09