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HRID 736694Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/736694

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
Edukt3-(1,3-Dioxolan-2-ylmethyl)benzoic acidHCID 24726992—
Edukt2,3-Diaminobenzamide dihydrochlorideHCID 53422807—
LösungsmittelPyridineHCID 1049—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(3-[1,3]dioxolan-2-ylmethylphenyl)-1H-benzimidazole-4-carboxamideHCID 68532968—

Reaktionsschritte

A solution of 3-(1,3-dioxolan-2-ylmethyl)benzoic acid (1.0 g, 4.80 mmol) in a mixture of 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 purified by flash chromatography on silica gel with 10% methanol in 2:1 ethyl acetate/hexane. The product was dissolved in acetic acid (20 mL) and the solution heated at 60° C. for 2 hours and at 80° C. for 1.5 hours, cooled and concentrated and the residue partitioned between ethyl acetate and sodium bicarbonate solution. The organic phase was concentrated and the residue purified on silica gel with 10% methanol in 2:1 ethyl acetate/hexane to give 1.13 g of the title compound. MS (APCI) m/z 324 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07595406B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-4f666f28f3d7411483a7b720ca25ab08
Quellennotizuspto-grants-2009_09