戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1609526作成日:2026年10月25日

Triethylamine → HCID 178441839、化合物

https://huagongshe.com/reaction/1609526

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Valeryl chlorideHCID 61186—
反応物2-Amino-5-methylbenzoic acidHCID 76255—
反応物Ethyl acetate hexaneHCID 21226206—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DimethylformamideHCID 6228—
生成物HCID 178441839HCID 17844183925%

反応条件

温度0 °C

反応手順

To a solution of 3.0 g (20 mmol) of 2-amino-5-methyl benzoic acid in 20 mL of dry DMF at 0° C. was added 200 mg of DMAP followed by 6.07 g (60 mmol) of triethylamine and 5.02 g (40 mmol) of valeryl chloride. The resulting mixture was stirred at 0° C. for 30 min. The mixture was heated to 110° C. and monitored by TLC for the formation of the intermediate quinoxazolone (Rf =0.8, 40% EtOAc/hexane). Following complete formation of the intermediate 10 g (100 mmol) of (NH4)2CO3 was added cautiously. Heating was continued to ensure consumption of the quinoxazolone and formation of the polar (Rf =0.4, 40% EtOAc/hexane) quinazolin-4(1H)-one. The reaction mixture was concentrated in vacuo and the residue was taken up in 50 mL of ether and 50 mL of water. The mixture was filtered and the filtrate discarded after washing the residue with 20 mL of ether. The residue was recrystalized from MeOH to give 1.07 g (25%) of the title compound as a white crystalline solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05401745
出典データセットuspto-grants-1995_03
ORD IDord-c212d50860dd4e1982e2f03aeb761ec5
出典メモuspto-grants-1995_03