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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461780Generated: October 30, 2026

Bromopinacolone → HCID 21392477, compound

https://huagongshe.com/reaction/461780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromopinacoloneHCID 21642—
Reactant4-prop-2-enylpiperazine-1-carbothioamideHCID 4740506—
SolventEthanolHCID 702—
ProductHCID 21392477HCID 21392477—

Reaction Steps

3.7 g of 4-allyl-1-piperazinyl-thiocarboxamide are added to a solution of 3.6 g of bromopinacoline in 40 cc of ethanol, and the reaction mixture is subsequently heated to the boil at reflux for 2 hours. The mixture is subsequently concentrated by evaporation in a vacuum, the residue is dissolved in a small amount of water and divided between ether and a concentrated aqueous sodium hydroxide solution. The ether phase is washed with water, dried over sodium sulphate and saturated with hydrogen chloride gas after filtration. The monohydrochloride of 2-(4-allyl-1-piperazinyl)-4-tert.butyl-thiazole crystallizes and has an M.P. of 212°-214° after recrystallization from ethanol/diisopropyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04064244
Source datasetuspto-grants-1977_12
ORD IDord-aeffb55f95fd41658204d7f3c3b97d7a
Source noteuspto-grants-1977_12