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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648981Generated: October 30, 2026

Pyridine → HCID 13649190, compound

https://huagongshe.com/reaction/648981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
Reactant1-BenzylpiperazineHCID 75994—
Reactant2-Oxindole-5-carboxylic acidHCID 2773318—
SolventDichloromethaneHCID 6344—
ProductHCID 13649190HCID 136491909%

Reaction Steps

To a suspension of 1.76 g of 5-carboxyoxindol in 200 ml of methylene chloride was added 2 ml of pyridine. After completion of addition, to the suspension was added dropwise 1.4 g of thionyl chloride with stirring held at 0° to 20° C. After completion of addition, the mixture was stirred at the same temperature for 1 hour, and a solution of 1.74 g of benzylpiperazine in 10 ml of methylene chloride was added dropwise thereto. The mixture was then stirred for 4 hours at room temperature. The reaction mixture was thoroughly washed with an aqueous potassium carbonate solution, then washed with water, and dilute hydrochloric acid, dried over sodium sulfate, and the solvent was distilled off. The residue was isolated and purified by silica-gel column chromatography [silica-gel: WAKO C-200, eluent: chloroform:methanol (V/V)=20:1] followed by recrystallization from isopropyl alcohol to give 298 mg of 5-(4-benzyl-1-piperazinylcarbonyl)oxindol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04737501
Source datasetuspto-grants-1988_04
ORD IDord-00651fbc754948d5b30720fd11d39c6e
Source noteuspto-grants-1988_04