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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383645Generated: October 25, 2026

4-(Pyrrolidin-1-yl)phenacyl bromide → HCID 59406739, compound

https://huagongshe.com/reaction/383645

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Pyrrolidin-1-yl)phenacyl bromideHCID 3681785—
ReactantEthyl[3-(6-oxo-3-thiocarbamoyl-6h-pyridazin-1-yl-methyl)phenyl]carbamateHCID 59406698—
SolventEthanolHCID 702—
ProductHCID 59406739HCID 59406739—

Reaction Conditions

Temperature80 °C

Reaction Steps

104 mg (0.31 mmol) of ethyl[3-(6-oxo-3-thiocarbamoyl-6H-pyridazin-1-yl-methyl)phenyl]carbamate are suspended in 2 ml of EtOH, and 100 mg (0.37 mmol) of α-bromo-4-(1-pyrrolidino)acetophenone are added. The reaction mixture is stirred at 80° C. for 15 h. The precipitate formed is filtered off with suction and washed with ethanol and dried in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367668B2
Source datasetuspto-grants-2013_02
ORD IDord-aa239a8cb89b42f0a6711a235c785e39
Source noteuspto-grants-2013_02