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HRID 430513作成日:2026年10月24日

O-Toluidine → 3-Aminopyrazine-2carboxylic acid o-toluamide

https://huagongshe.com/ja/reaction/430513

反応式

関与物質

役割名称HCID仕込み量
反応物O-ToluidineHCID 7242—
反応物3-Amino-2-pyrazinecarboxylic acidHCID 72656—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物3-Aminopyrazine-2carboxylic acid o-toluamideHCID 69709687—

反応手順

A mixture of 3-aminopyrazine carboxylic acid (5.0 g, 35.94 mmol), methylene chloride (110 mL), 4-dimethylaminopyridine (10.98 g, 89.85 mmol), o-toluidine (4.22 mL, 39.53 mmol), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (8.27 g, 43.13 mmol) was stirred overnight at ambient temperature. The solvent was removed and the residue was diluted with ethyl acetate. This organic phase was extracted with 1N lithium chloride (LiCl), water, and brine, dried over calcium sulfate and concentrated. The residue was flash chromatographed on silica gel (2.75×4 inches) with elution proceeding as follows: hexane (300 mL), nil; 20% ethyl acetate/hexane (500 mL), unweighed recovered o-toluidine; 20% ethyl acetate/hexane (1000 mL) and 30% ethyl acetate/hexane (2000 mL), 4.79 g (58%) of 3-aminopyrazine-2-carboxylic acid o-toluamide as a yellow crystalline solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06323208B1
出典データセットuspto-grants-2001_11
ORD IDord-30b50b024d454e2f9097c902eda62b64
出典メモuspto-grants-2001_11