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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649236Generated: October 31, 2026

Allyl chloride → HCID 70536330, compound

https://huagongshe.com/reaction/1649236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chlorideHCID 7850—
ReactantSodium amideHCID 24533—
ReactantHCID 13236333HCID 13236333—
SolventDimethylformamideHCID 6228—
ProductHCID 70536330HCID 70536330119.8%

Reaction Steps

5-[4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril (1.96 g) and 0.20 g of sodium amide were mixed with 60 ml of DMF and stirred at room temperature for 2 hours. Then, to the mixture was added 0.67 g of allyl chloride and the mixture was stirred at room temperature for 10 hours. The reaction mixture was poured into 150 ml of saturated saline solution and organic substances were extracted with chloroform. The chloroform layer was washed with water and dehydrated. Chloroform was distilled off and the residue was purified through silica gel column chromatography followed by recrystallization from methanol-ether to give 1.76 g of 1-allyl-5-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril hemihydrate, m.p. 120°-122° C., colorless granules.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04415572
Source datasetuspto-grants-1983_11
ORD IDord-f328352f54984c88baa18bac7314dec4
Source noteuspto-grants-1983_11