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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648980Generated: October 29, 2026

Trimethylamine → HCID 13649190, compound

https://huagongshe.com/reaction/648980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylamineHCID 1146—
ReactantDiethyl chlorophosphateHCID 13139—
Reactant1-BenzylpiperazineHCID 75994—
Reactant2-Oxindole-5-carboxylic acidHCID 2773318—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13649190HCID 1364919057.4%

Reaction Steps

5-Carboxyoxindol (0.93 g) and 0.8 ml of trimethylamine were suspended in 10 ml of tetrahydrofuran (THF), and a solution of 1.0 g of diethylchlorophosphate in 10 ml of THF was added dropwise thereto at room temperature with stirring. The mixture was stirred for 3 hours at room temperature. To the mixture was added dropwise a solution of 1.1 g of benzylpiperazine in 10 ml of THF and was further stirred for 10 hours at room temperature. After completion of reaction, crystals which precipitated were filtered off and the filtrate was concentrated. To the residue was added a saturated aqueous solution of sodium hydrogencarbonate and the mixture was extracted with chloroform. Organic layer was washed with water and a saturated saline solution, dried over anhydrous sodium sulfate, and the solvent was distilled off. Recrystallization of the residue from isopropyl alcohol gave 1.01 g of 5-(4-benzyl-1-piperazinylcarbonyl)oxindol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04737501
Source datasetuspto-grants-1988_04
ORD IDord-1f42e14d392f4ad1bbe108c5e3bb8488
Source noteuspto-grants-1988_04