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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3645생성일: 2026년 10월 23일

Dimethylformamide → 5-(2-Ethoxybenzamido)-1-n-propylimidazole-4-carboxamide

https://huagongshe.com/ko/reaction/3645

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Oxalyl chlorideHCID 65578—
반응물2-Ethoxybenzoic acidHCID 67252—
반응물5-Amino-1-propyl-1H-imidazole-4-carboxamideHCID 12339105—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물5-(2-Ethoxybenzamido)-1-n-propylimidazole-4-carboxamideHCID 5371330977%

반응 단계

Oxalyl chloride (1.74 g, 0.137 mol) was added dropwise to a stirred solution of 2-ethoxybenzoic acid (1.1 g, 0.00663 mol) and dimethylformamide (0.1 ml) in dichloromethane (20 ml) and the resulting mixture stirred at ambient temperature for 4 hours, then evaporated under vacuum. The residue was azeotroped with dichloromethane (2×20 ml), then added dropwise to a stirred solution of 5-amino-1-n-propylimidazole-4-carboxamide (0.9 g, 0.00536 mol) in pyridine (20 ml) The resulting solution was stirred at ambient temperature for 3 days, then evaporated under vacuum. The residue was dissolved in dichloromethane (50 ml), and the solution washed with 1N hydrochloric acid (30 ml), dried (Na2SO4) and evaporated under vacuum. Chromatography of the crude product on silica gel (15 g) using a methanol in dichloromethane elution gradient (2-6% methanol), followed by crystallisation from ethanol, gave the title compound as a colourless solid (1.3 g, 77%), m.p. 182°-184° C. Found: C,60.85; H,6.40; N,18.06. C16H20N4O3 requires C,60.74; H,6.37; N,17.71%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05734053
출처 데이터셋uspto-grants-1998_03
ORD IDord-7a5e2995d24f4bac852bdb664f6ad601
출처 메모uspto-grants-1998_03