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HRID 49530作成日:2026年10月24日

Hydrogen Bromide → 5-(2-bromo-2-carbamoylethyl)-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide

https://huagongshe.com/ja/reaction/49530

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen BromideHCID 260—
反応物AcrylamideHCID 6579—
反応物5-amino-2-methoxy-N-(4-trifluoromethylbenzyl)benzamideHCID 10903424—
反応物Sodium NitriteHCID 23668193—
溶媒AcetoneHCID 180—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物5-(2-bromo-2-carbamoylethyl)-2-methoxy-N-(4-trifluoromethylbenzyl)benzamideHCID 12094663—

反応条件

温度30 °C

反応手順

To a solution of 2.26 g of 5-amino-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide in 27 ml of acetone and 11 ml of methanol were added 5.6 ml of 47% solution of hydrobromic acid, 540 mg of sodium nitrite and 2 ml of water under cooling with ice, and the mixture was stirred for 10 minutes. To the reaction mixture were added 3.00 g of acrylamide, and, after heated to 30° C., 135 mg of cupric oxide were added little by little, and the mixture was stirred further for 2 hours at 30° C. Solvent was distilled off under reduced pressure, and 25% aqueous ammonia was added to the residue, which was extracted with ethyl acetate. The organic layer was washed with water and saturated brine in sequence and dried over anhydrous sodium sulfate. Solvent was distilled off under reduced pressure, the residue obtained was crystallized from hexane:ethyl acetate=1:1, and then the crystals were collected by filtration to obtain 1.55 g of 5-(2-bromo-2-carbamoylethyl)-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide as colorless crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06706763B1
出典データセットuspto-grants-2004_03
ORD IDord-166dbfddd38c4b35b4a216d8319fea93
出典メモuspto-grants-2004_03