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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648973Generated: October 26, 2026

Water → 5-[4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]oxindol

https://huagongshe.com/reaction/648973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantVeratroyl chlorideHCID 77070—
Reactant5-(1-Piperazinyl)oxindol.hydrobromideHCID 13646031—
SolventDimethylformamideHCID 6228—
Product5-[4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]oxindolHCID 1364603258.6%

Reaction Steps

5-(1-Piperazinyl)oxindol.hydrobromide (2.0 g) was suspended in 30 ml of N,N-dimethylformamide (DMF), and 2.3 ml of triethylamine was added thereto subsequently. The mixture was cooled to 0° to 5° C. To the mixture was added dropwise 5 ml of DMF solution containing 1.5 g of 3,4-dimethoxybenzoyl chloride at the same temperature as above with stirring. After completion of addition, the mixture was stirred at room temperature for one hour. The reaction mixture was poured into a large amount of water and extracted with chloroform. After washing with water, the extract was dried over anhydrous sodium sulfate and chloroform was removed by distillation. The residue was purified by silica-gel column chromatography (eluent: chloroform:methanol=100:1) and recrystallized from methanol to give 1.5 g of 5-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]oxindol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04737501
Source datasetuspto-grants-1988_04
ORD IDord-dfe06f226bbe4c7c89f875369a1139db
Source noteuspto-grants-1988_04