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HRID 722410作成日:2026年10月23日

Hydrochloric Acid → N-[4-(2-carbamoyl-ethylamino)-3-nitro-phenyl]-N-methyl-benzamide

https://huagongshe.com/ja/reaction/722410

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物DiisopropylethylamineHCID 81531—
反応物Benzamide, N-(4-fluoro-3-nitrophenyl)-N-methyl-HCID 11460004—
反応物3-Aminopropanamide hydrochlorideHCID 22222288—
溶媒AcetonitrileHCID 6342—
生成物N-[4-(2-carbamoyl-ethylamino)-3-nitro-phenyl]-N-methyl-benzamideHCID 21884188—

反応条件

温度80 °C

反応手順

N-(4-fluoro-3-nitro-phenyl)-N-methyl-benzamide (1.47 g, 5.37 mmol) was taken up in dry acetonitrile under argon, DIEA (2.08 g, 16.11 mmol, 2.80 ml) and β-alanine amide hydrochloride (1.00 g, 8.06 mmol) were added. The reaction mixture was heated to 80° C. for 48 h. The reaction was poured into 1N HCl and the aqueous layer was extracted 3× with ethyl acetate. The combined organic layers were washed with water, brine and dried over magnesium sulfate. The solution was filtered and the solvent removed under reduced pressure. The residue was triturated twice with cold hexane and dried to give N-[4-(2-carbamoyl-ethylamino)-3-nitro-phenyl]-N-methyl-benzamide. (1.75 g, 95%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07138420B2
出典データセットuspto-grants-2006_11
ORD IDord-e834417c845e47c1acbbc78398a6df70
出典メモuspto-grants-2006_11