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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 430513생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/430513

반응식

참여 물질

역할이름HCID투입량
반응물O-ToluidineHCID 7242—
반응물3-Amino-2-pyrazinecarboxylic acidHCID 72656—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물3-Aminopyrazine-2carboxylic acid o-toluamideHCID 69709687—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06323208B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-30b50b024d454e2f9097c902eda62b64
출처 메모uspto-grants-2001_11