Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278126Generated: November 1, 2026

2-Chlorobenzoyl chloride → HCID 22627283, compound

https://huagongshe.com/reaction/278126

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzoyl chlorideHCID 69110—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 22627421HCID 22627421—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 22627283HCID 22627283115.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a stirred mixture of benzyl 3-isobutyryl-2-propylindole-6-carboxylate (207 mg) and diisopropylethylamine (295 mg) in dichloromethane (6 ml) were added 2-chlorobenzoyl chloride (299 mg) and 4-dimethylaminopyridine (12 mg) at 0° C. The reaction mixture was refluxed for 15 hours. The reaction mixture was cooled to 20° C. and washed with 1N hydrochloric acid, water, saturated sodium bicarbonate, water and brine. The organic phase was dried over sodium sulfate and evaporated in vacuo. The residue was chromatographed or silica gel eluting with a mixture of ethyl acetate and hexane (1:10) to give benzyl 1-(2-chlorobenzoyl)-3-isobutyryl-2-propylindole-6-carboxylate (330 mg) as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358992B1
Source datasetuspto-grants-2002_03
ORD IDord-5bc2c9462baf478e857abda514d5ee6f
Source noteuspto-grants-2002_03