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HRID 339880作成日:2026年10月26日
Tetraethyl orthocarbonate → 5-(3-Bromophenyl)-2-ethoxy-5-fluoro-6,6-dimethyl-5,6-dihydro-1,4,3-oxathiazine 4,4-dioxide
https://huagongshe.com/reaction/339880
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetraethyl orthocarbonate | HCID 66213 | — |
| 反応物 | HCID 68292393 | HCID 68292393 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 5-(3-Bromophenyl)-2-ethoxy-5-fluoro-6,6-dimethyl-5,6-dihydro-1,4,3-oxathiazine 4,4-dioxide | HCID 68359207 | — |
反応手順
A mixture of 75 mg of 1-(3-bromophenyl)-1-fluoro-2-hydroxy-2-methylpropane-1-sulfonamide in 5 ml of tetraethoxymethane and 1 ml of acetic acid was stirred at 100° C. for 1.5 hours. The conversion was checked by LCMS. Since it was incomplete, the reaction mixture was stirred at 100° C. for a further 3.5 hours. After the removal of the solvents under reduced pressure, the residue was purified by means of normal phase chromatography using a Flashmaster with an n-heptane/ethyl acetate gradient. The product-containing fractions were combined and concentrated by rotary evaporation. This gave the product (45.6 mg) with a molecular weight of 380.2 g/mol (C13H15BrFNO4S).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08895547B2 |
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| 出典データセット | uspto-grants-2014_11 |
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| ORD ID | ord-9bfd0b628c204c6d95b22f944706bc75 |
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| 出典メモ | uspto-grants-2014_11 |
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