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HRID 79093作成日:2026年10月23日

Benzenesulfonamide, 3-amino- → 2-(4-Fluorophenoxy)-4-tert-butyl-N-(3-(aminosulfonyl)phenyl)benzamide

https://huagongshe.com/ja/reaction/79093

反応式

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 ChlorideHCID 24386—
反応物2-(4-Fluorophenoxy)-4-tert-butylbenzoic acidHCID 58988089—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物2-(4-Fluorophenoxy)-4-tert-butyl-N-(3-(aminosulfonyl)phenyl)benzamideHCID 2485521150%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841483B2
出典データセットuspto-grants-2014_09
ORD IDord-9f3311df790543d0b65bf661b6c85066
出典メモuspto-grants-2014_09