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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912661Generated: October 26, 2026

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

https://huagongshe.com/reaction/912661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant5-Aminoimidazole-4-carboxamideHCID 9679—
Reactant2-Butyl-5-chloro-1H-imidazole-4-carbaldehydeHCID 55176—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
Product4-{[(2-Butyl-4-chloro-1H-imidazol-5-yl)methyl]amino}-1H-imidazole-5-carboxamideHCID 6741416126%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026244B2
Source datasetuspto-grants-2011_09
ORD IDord-ef92e652f2bb4a359c25e63cdfca4f47
Source noteuspto-grants-2011_09