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HRID 1914487作成日:2026年10月27日

Niclosamide → 4-Chloro-2-(2-chloro-4-nitrophenylcarbamoyl)phenyl benzoate

https://huagongshe.com/reaction/1914487

反応式

関与物質

役割名称HCID仕込み量
反応物NiclosamideHCID 4477—
反応物Benzoyl chlorideHCID 7412—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒PyridineHCID 1049—
生成物4-Chloro-2-(2-chloro-4-nitrophenylcarbamoyl)phenyl benzoateHCID 23966630—

反応条件

温度50 °C

反応手順

A suspension of 5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide (1.27 g., 3.88 mmol) in pyridine (15 mL) was treated with 4-dimethylaminopyridine (30 mg) and benzoyl chloride (0.49 mL, 4.27 mmol) was introduced dropwise. The suspension was warmed to 50° C. for one hour then cooled to room temperature and stirred for 17 hours. The reaction mixture was partitioned between 1N aqueous HCl and ethyl acetate. The ethyl acetate phase was washed with water, then brine, dried over magnesium sulfate, and concentrated to an off-white solid. This was recrystallized from ethyl acetate/hexanes. 1HNMR (500 MHz, DMSO-d6): δ7.70 (M, 3H), 7.73 (m, 2H), 7.89 (m, 1H), 7.93 (M, 1H), 8.19 (m, 1H), 8.32 (m, 1H), 10.60 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08614205B2
出典データセットuspto-grants-2013_12
ORD IDord-ff01bf9a2af444e6adce3addbdef6caf
出典メモuspto-grants-2013_12