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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263473Generated: October 30, 2026

Water → HCID 18616321, compound

https://huagongshe.com/reaction/1263473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Aminobenzoic AcidHCID 978—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant4-BenzylpiperidineHCID 31738—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductHCID 18616321HCID 1861632151.8%

Reaction Steps

4-Aminobenzoic acid (1.61g, 10 mM) was reacted with EDAC (1.92g, 10 mM) in 40 mL dry DMF for 15 minutes. 4-Benzylpiperidine (1.75g, 10 mM) was added followed by DMAP (20 mg, catalyst) and the reaction mixture was stirred for 20 h. The mixture was poured into water and extracted with methylene chloride (3×100 mL). The combined extract was washed with dilute hydrochloric acid, saturated sodium bicarbonate and water and dried over MgSO4. After evaporation of the solvent, the residue was chromatographed with methylene chloride-methanol (0 to 2% methanol, gradient) to yield 1.60 g (50%) of the title compound after recrystallization from ether-Hexane. 1H NMR (CDCl3): δ 7.40-7.10 (m, 7H), 6.70 (d, 2H), 3.95-3.90 (broad m, 2H), 2.85-2.75 (broad m, 2H), 2.6 (d, 2H), 1.85-1.80 (m, 1H), 2.75-2.65 (broad m, 2H), 1.15-1.05 (broad m, 2H). MS (ESI) m/e 294 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541477B2
Source datasetuspto-grants-2003_04
ORD IDord-7a418637f1954e9094a10593d1a7ff14
Source noteuspto-grants-2003_04