関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzenesulfonamide, 3-amino- | HCID 7377 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | 2-(4-Fluorophenoxy)-4-tert-butylbenzoic acid | HCID 58988089 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-(4-Fluorophenoxy)-4-tert-butyl-N-(3-(aminosulfonyl)phenyl)benzamide | HCID 24855211 | 50% |
反応手順
A solution of 2-(4-fluorophenoxy)-4-tert-butylbenzoic acid (0.11 g, 0.39 mmol) and thionyl chloride (0.28 mL, 3.9 mmol) in CH2Cl2 (10 mL) was stirred at room temperature for 4 h. The solvent was evaporated under reduced pressure, and to the resulting oil was added a solution of 3-amino-benzenesulfonamide (73 mg, 0.42 mmol) in pyridine (4 mL). The solution was stirred at room temperature 15 h. The reaction was diluted with water and extracted with EtOAc. The combined extracts were washed with water, dried over Na2SO4, and evaporated under reduced pressure. The residue was purified by silica gel chromatography (0%-50% EtOAc-hexanes) to obtain a white solid which was recrystallized from EtOAc and hexanes. 2-(4-Fluorophenoxy)-4-tert-butyl-N-(3-(aminosulfonyl)phenyl)benzamide (85 mg, 50% yield) was obtained as a white solid. LC/MS: m/z 443.3 (M+H)+ at 3.49 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08841483B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-9f3311df790543d0b65bf661b6c85066 |
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| 出典メモ | uspto-grants-2014_09 |
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