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HRID 349476作成日:2026年10月27日

p-Toluenesulfonic acid → 3-[(2,4-dichloro-N-chloro-benzimidoyl)-amino]-4-methoxy-benzoic acid methyl ester

https://huagongshe.com/reaction/349476

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物2,4-DichlorobenzonitrileHCID 81050—
反応物Sodium BicarbonateHCID 516892—
反応物Methyl 3-Amino-4-methoxybenzoateHCID 2734814—
反応物Sodium HypochloriteHCID 23665760—
生成物3-[(2,4-dichloro-N-chloro-benzimidoyl)-amino]-4-methoxy-benzoic acid methyl esterHCID 6911973384%

反応条件

温度180 °C

反応手順

Anhydrous p-toluene sulfonic acid (20.99 g, 110.04 mmol) was melted at 120° C. and 3-amino-4-methoxy benzoic acid methyl ester (10 g, 55.20 mmol) obtained in step 1 of Preparation Example 1 and 2,4-dichlorobenzonitrile (18.99 g, 110.04 mol) were added thereto and stirred at 180° C. for 6 hours. The resulting solution was cooled to room temperature and the reaction was stopped by adding NaHCO3 thereto. The resulting mixture was extracted with ethyl acetate, the extract was dried over MgSO4 and concentrated under a reduced pressure. The concentrate was dissolved in 50% methanol and 5% NaOCl (30 ml, 20.64 mmol) was added dropwise thereto. After 5 min, the resulting mixture was extracted with ethyl acetate, the extract was dried over MgSO4 and concentrated under a reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent—MeOH:CDCl3=5:95, Merck, Silicagel 60) to obtain the title compound (18 g, 10.32 mmol) in a yield of 84%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07179832B2
出典データセットuspto-grants-2007_02
ORD IDord-3577b128423d43f1b30b6d9e0ebc0a93
出典メモuspto-grants-2007_02