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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842028Generated: October 30, 2026

Hydrochloric Acid → Piperidine,4-(4-chlorobenzoyl)-1-(1h-indol-5-ylcarbonyl)-

https://huagongshe.com/reaction/842028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1H-Indole-5-Carboxylic AcidHCID 74280—
Reactant4-(4-Chlorobenzoyl)piperidine hydrochlorideHCID 2777114—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductPiperidine,4-(4-chlorobenzoyl)-1-(1h-indol-5-ylcarbonyl)-HCID 9947354—

Reaction Steps

Indole-5-carboxylic acid (18 mg, 0.11 mmole) and 4-(4-chlorobenzoyl) piperidine hydrochloride (26 mg, 0.1 mmole) were dissolved in 5 ml dichloromethane. To this solution was added triethylamine (1 eq. to neutralize the HCl salt) catalytic DMAP and EDCI (33 mg, 0.11 mmole). The reaction mxture was stirred at room temperature overnight and then worked up by washing sequentially with 1N HCl, saturated sodium bicarbonate, and saturated sodium chloride. The compound was then purified by flash chromatography on silica gel (40:1 CHCl3/MeOH). 1H NMR (300 Mhz, CDCl3) δ 8.45 (s, 1H), 7.88 (d, 2H), 7.72 (s, 1H), 7.45 (d, 2H), 7.38 (d, 1H), 7.24 (s, 2H), 6.58 (s, 1H), 3.42 (m, 1H), 3.11 (m, 2H), 1.83 (m, 4H), 1.60 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372752B1
Source datasetuspto-grants-2002_04
ORD IDord-8309e2d0af0a44819c6f8016f8449903
Source noteuspto-grants-2002_04