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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673145Generated: October 30, 2026

1,1'-Carbonyldiimidazole → 2-(4-[1,3]-Dioxolan-2-ylmethylphenyl)-1H-benzimidazole-4-carboxamide

https://huagongshe.com/reaction/1673145

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4-(1,3-Dioxolan-2-ylmethyl)benzoic acidHCID 24726991—
Reactant2,3-Diaminobenzamide dihydrochlorideHCID 53422807—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
Product2-(4-[1,3]-Dioxolan-2-ylmethylphenyl)-1H-benzimidazole-4-carboxamideHCID 67353248—

Reaction Steps

A solution of 4-(1,3-dioxolan-2-ylmethyl)benzoic acid (1.0 g, 4.80 mmol) in pyridine (5 mL) and N,N-dimethylformamide (5 mL) was treated with 1,1′-carbonyldiimidazole (0.856 g, 5.28 mmol) at 45° C. for 2 hours. 2,3-Diaminobenzamide dihydrochloride (synthesized as described in U.S. Pat. No. 6,737,421, column 11, EXAMPLE 2, step (e), 1.08 g, 4.80 mmol) was added and the mixture stirred at ambient temperature overnight. The mixture was concentrated and the residue heated in acetic acid (30 mL) at 80° C. for 3 hours. After cooling, the mixture was concentrated and the residue partitioned between ethyl acetate and sodium bicarbonate solution. After filtering, the filtrate was concentrated and the residue purified by flash chromatography on silica gel (0-15% methanol in 2:1 ethyl acetate/hexane) to give 1.14 g of the title compound. MS (DCI) m/z 324 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999117B2
Source datasetuspto-grants-2011_08
ORD IDord-2fe37a1f41394aca875be80c8390741f
Source noteuspto-grants-2011_08