Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649211Generated: October 31, 2026

Water → 5-[4-(4-Methoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/1649211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Anisoyl chlorideHCID 7477—
ReactantTriethylamineHCID 8471—
Reactant5-(1-Piperazinyl)-3,4-dihydrocarbostyril monohydrobromideHCID 20480591—
SolventDimethylformamideHCID 6228—
Product5-[4-(4-Methoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyrilHCID 1323634236.1%

Reaction Steps

5-(1-Piperazinyl)-3,4-dihydrocarbostyril monohydrobromide (2.6 g) and 2.34 ml of triethylamine were dissolved in 40 ml of DMF. The mixture was stirred at room temperature while slowly adding dropwise 10 ml of DMF solution containing 2.5 g of 4-methoxybenzoyl chloride. After completion of addition the reaction mixture was stirred for 30 minutes. The reaction mixture was poured into a large amount of water and extracted with chloroform. The extract was washed with saturated sodium hydrogencarbonate solution and subsequently with water and dried over anhydrous sodium sulfate. Chloroform was distilled off and residual crystals were recrystallized from methanol-chloroform to give 1.1 g of 5-[4-(4-methoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril, m.p. 219°-220° C., colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04415572
Source datasetuspto-grants-1983_11
ORD IDord-b96a25f375e547de96f3ce2f53ef1fdd
Source noteuspto-grants-1983_11