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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 912661생성일: 2026년 10월 27일

Acetic Acid → 4-{[(2-Butyl-4-chloro-1H-imidazol-5-yl)methyl]amino}-1H-imidazole-5-carboxamide

https://huagongshe.com/reaction/912661

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물5-Aminoimidazole-4-carboxamideHCID 9679—
반응물2-Butyl-5-chloro-1H-imidazole-4-carbaldehydeHCID 55176—
반응물Sodium cyanoborohydrideHCID 5003444—
용매MethanolHCID 887—
생성물4-{[(2-Butyl-4-chloro-1H-imidazol-5-yl)methyl]amino}-1H-imidazole-5-carboxamideHCID 6741416126%

반응 단계

A reaction mixture of 4-amino-5-imidazolecarboxamide (0.50 g, 3.96 mmol), 2-butyl-5-chloro-1H-imidazole-4-carbaldehyde (0.89 g, 4.76 mmol), and NaCNBH3 (0.25 g, 3.96 mmol) in methanol (5 mL) was stirred at r.t. over night. Acetic acid (0.24 g, 3.96 mmol) was added and the mixture was heated at 50° C. for 5 h. The mixture was concentrated in vacuo and dissolved in ethyl acetate and washed with water. The aqueous phase was extracted twice with ethyl acetate. The combined organic layers were dried (MgSO4) and concentrated. The crude product was purified by flash column chromatography (CH2Cl2/methanol gradient; 0 to 20% methanol), obtaining 0.30 g (26%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08026244B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-ef92e652f2bb4a359c25e63cdfca4f47
출처 메모uspto-grants-2011_09