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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374685Generated: October 31, 2026

1,1'-Carbonyldiimidazole → 2-(4-[1,3] Dioxolan-2-yl-2-fluorophenyl)-1h-benzimidazole-4-carboxamide

https://huagongshe.com/reaction/2374685

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2,3-Diaminobenzamide dihydrochlorideHCID 53422807—
Reactant4-(1,3-Dioxolan-2-yl)-2-fluorobenzoic acidHCID 67353916—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
Product2-(4-[1,3] Dioxolan-2-yl-2-fluorophenyl)-1h-benzimidazole-4-carboxamideHCID 6735295222%

Reaction Steps

A solution of EXAMPLE 20D (1.5 g, 7.1 mmol) in pyridine (5 mL) and N,N-dimethylformamide (20 mL) was treated with 1,1′-carbonyldiimidazole (1.4 g, 8.5 mmol) at 40° C. for 30 minutes. 2,3-Diaminobenzamide dihydrochloride (synthesized as described in U.S. Pat. No. 6,737,421, column 11, EXAMPLE 2, step (e), 1.58 g, 7.1 mmol) was added and the mixture stirred at ambient temperature overnight. Solvents were removed and the residue suspended in 10 mL of acetic acid. The mixture was stirred at 80° C. overnight, cooled, and concentrated and the residue was purified by flash chromatography using ethyl acetate to give the title compound (500 mg, 22%). MS (DCI/NH3) m/z 329 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462724B2
Source datasetuspto-grants-2008_12
ORD IDord-0941408ce7024a47a935ba4d6ca7afc6
Source noteuspto-grants-2008_12