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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250839Generated: October 29, 2026

Water → HCID 54031537, compound

https://huagongshe.com/reaction/1250839

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 (˜20mg, 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 numberUS06340685B1
Source datasetuspto-grants-2002_01
ORD IDord-6db0b1ed56aa4d78a4b5434e1bd91e25
Source noteuspto-grants-2002_01