戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 20140作成日:2026年10月23日

Methanol → tert-Butyl (3R,6S)-6-(2,3-difluorophenyl)-1-[2-(methylsulfonyl)ethyl]-2-oxoazepan-3-ylcarbamate

https://huagongshe.com/ja/reaction/20140

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Potassium hydroxy sulfiteHCID 23707502—
反応物tert-butyl (3R,6S)-6-(2,3-difluorophenyl)-1-[2-(methylthio)ethyl]-2-oxoazepan-3-ylcarbamateHCID 86595038—
溶媒WaterHCID 962—
生成物tert-Butyl (3R,6S)-6-(2,3-difluorophenyl)-1-[2-(methylsulfonyl)ethyl]-2-oxoazepan-3-ylcarbamateHCID 86595040—

反応手順

Oxone® ((16.1 mg, 0.11 mmol) was added to a solution of tert-butyl (3R,6S)-6-(2,3-difluorophenyl)-1-[2-(methylthio)ethyl]-2-oxoazepan-3-ylcarbamate (22 mg, 0.053 mmol) in methanol (2 mL) and water (2 mL). After 6 h excess oxone (32 mg, 0.22 mmol) was added. After 18 h, the reaction was quenched with aqueous sodium sulfite solution and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium carbonate (3×), saturated brine, dried over magnesium sulfate, filtered and concentrated to give the title compound. MS 447 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745427B2
出典データセットuspto-grants-2010_06
ORD IDord-87541fac1f3341f8b17e1ec1523c152f
出典メモuspto-grants-2010_06