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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736701Generated: October 28, 2026

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

https://huagongshe.com/reaction/736701

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 numberUS07595406B2
Source datasetuspto-grants-2009_09
ORD IDord-c493b24ff334458da3f0b13a2aaa3ae1
Source noteuspto-grants-2009_09