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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842475Generated: November 3, 2026

1,1'-Carbonyldiimidazole → HCID 178419323, compound

https://huagongshe.com/reaction/1842475

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4-Bromobenzene-1,2-diamineHCID 323593—
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
ProductHCID 178419323HCID 17841932360.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

To the mixture of piperidine-1,4-dicarboxylic acid mono-tert-butyl ester (2 g, 8.7 mmol) in DMF (15 mL) and pyridine (15 mL) was added CDI (1.55 g, 9.57 mmol) at 45° C. and the mixture was stirred for another 2 h at this temperature. Then 4-Bromo-benzene-1,2-diamine (1.63 g, 8.7 mmol) was added and the mixture was stirred at RT overnight. Solvents were removed in vacuo and the residue was dissolved in HOAc (10 mL) and heated for 1 h at 100° C. Then the reaction mixture was concentrated and the residue was partitioned between DCM and aqueous of Na2CO3. The organic layer was dried over Na2SO4 and concentrated to give the crude product which was purified by column chromatography (ethyl acetate:petroleum ether=1:2) to give the compound 5-Bromo-2-piperidin-4-yl-1H-benzoimidazole (1.47 g, 55%) as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946230B2
Source datasetuspto-grants-2015_02
ORD IDord-a7ff5ac41d1b44cf9dd814daabd435c1
Source noteuspto-grants-2015_02