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HRID 547520作成日:2026年10月27日

Water → 2-acetamido-N-(4-nitrophenyl)benzamide

https://huagongshe.com/reaction/547520

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-NitroanilineHCID 7475—
反応物3-Acetamidobenzoic acidHCID 48847—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物2-acetamido-N-(4-nitrophenyl)benzamideHCID 335331455%

反応条件

温度57.5 °C

反応手順

A mixture of 3-acetamidobenzoic acid (C1) (5.30 g, 29.58 mmol) and CDI (5.75 g, 35.50 mmol, 1.2 equivalent) in N-methylpyrrolidinone (20 mL) was heated at 55-60° C. for 2 h. 4-Nitroaniline (6.13 g, 44.37 mmol, 1.5 equivalent) was then added and the mixture was heated to 140° C. for 4 h, then poured into water (400 mL) and stirred for 18 h. The resulting precipitate was filtered and washed sequentially with water and CH2Cl2 and then crystallized from MeOH to give C2 (4.84 g; 55%) as a yellow solid; mp (MeOH) 259-261° C.; 1H NMR [(CD3)2SO] δ 10.80 (s, 1 H, NH), 10.15 (s, 1 H, NH), 8.29 (m, 2 H, H-{acute over (3)}& H-{acute over (5)}), 8.12 (t, J=1.8 Hz, 1 H, H-2), 7.84 (br dd, J=8.1, 1.2 Hz, 1 H, H-6), 7.65 (td, J=7.8, 2.5 Hz, 1 H, H-4), 7.48 (t, J=7.9 Hz, 1 H, H-5), 2.08 (s, 3H, COCH3); Anal. Calc. For C15H13N3O4: C, 60.2; H, 4.4; N, 14.0; found C, 60.4; H, 4.6; N, 14.1%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07939546B2
出典データセットuspto-grants-2011_05
ORD IDord-98575b1f5f1c4b22bb9bf237dcaca054
出典メモuspto-grants-2011_05