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HRID 32288作成日:2026年10月25日

Dichloromethane → N-(2-diethylamino-ethyl)-4-(2-benzyloxy-acetylamino)-2-methoxy-benzamide

https://huagongshe.com/reaction/32288

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物4-Amino-N-[2-(diethylamino)ethyl]-2-methoxybenzamideHCID 77374—
反応物(Benzyloxy)acetic acidHCID 290301—
溶媒WaterHCID 962—
生成物N-(2-diethylamino-ethyl)-4-(2-benzyloxy-acetylamino)-2-methoxy-benzamideHCID 5979333727%

反応条件

温度4 °C

反応手順

664 mg (4 mmol) of benzyloxyacetic acid is introduced into 20 ml of methylene chloride, mixed with 768 mg (4 mmol) of N′-(3-dimethylaminopropyl)-N-ethylcarbodiimide (EDG), and stirred for 0.5 hour at 4° C. Then, 1.06 g (4 mmol) of 4-amino-N-(2-diethylamino-ethyl)-2-methoxy-benzamide in a total of 12 ml of methylene chloride is added to the batch and stirred for 48 hours at room temperature. After 30 ml of water is added, it is extracted twice with 30 ml each of methylene chloride. The organic phase is dried, filtered and concentrated by evaporation. The residue is chromatographed on 20 g of Isolute NH2 (50 μm) with methylene chloride. The correspondingly combined fractions are concentrated by evaporation and chromatographed again on 20 g of Isolute NH2 (50 μm) with a gradient from cyclohexane to cyclohexane:methylene chloride=50:50 as an eluant, and 348 mg (27% of theory) of N-(2-diethylamino-ethyl)-4-(2-benzyloxy-acetylamino)-2-methoxy-benzamide is obtained as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07427390B2
出典データセットuspto-grants-2008_09
ORD IDord-82caffa4065a4ce5a8a0b285a7b56e7f
出典メモuspto-grants-2008_09