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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357040Generated: November 1, 2026

Water → HCID 54031537, compound

https://huagongshe.com/reaction/1357040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant4-BenzylpiperidineHCID 31738—
Reactant5-Benzimidazolecarboxylic acidHCID 459456—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductHCID 54031537HCID 5403153747%

Reaction Steps

Benzimidazole-5-carboxylic acid (1.62 g, 10 mMol) was reacted with EDAC (1.92 g, 10 mMol) in 40 mL dry DMF at room temperature for 15 minutes. To the reaction mixture was added 4-benzylpiperidine (1.75 g, 10 mMol) and DMAP (˜20 mg, catalyst) and the mixture was stirred at room temperature for 20 h. It was poured into water and extracted with methylene chloride (3-100 mL). The combined extract was washed with water, brine and again with water. The extract was dried over MgSO4 and evaporated. The residue was chromatographed on a column of silica gel with chloroform-methanol (0 to 5% methanol). Evaporation of the desired fractions gave 1.5 g (47%) of the product after recrystallization from ethyl acetate-hexane. 1HNMR (CDCl3): δ=7.8 (s, 1H); 7.1-7.3 (m, 8H); 4.8-4.7 (broad m, 1H), 3.7-3.9 (broad m, 1H); 3.1-2.7 (broad m, 2H); 2.55 (d, 2H); 2.0-1.1 (m, 5H). MS (ESI) m/e 319 (M+), 318 (M+−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06589954B1
Source datasetuspto-grants-2003_07
ORD IDord-812001bcf013403cbc8c524602a42f99
Source noteuspto-grants-2003_07