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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635355Generated: October 31, 2026

Ethanol → HCID 21258516, compound

https://huagongshe.com/reaction/635355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthylenethioureaHCID 2723650—
ReactantHCID 21258466HCID 21258466—
SolventAcetic AcidHCID 176—
ProductHCID 21258516HCID 21258516—

Reaction Steps

A mixture of the crude 2-bromo-1-[1-(4-chlorophenyl)cyclobutyl]-3-phenylpropan-1-one described above, imidazolidine-2-thione (1.02 g), ethanol (15 ml) and acetic acid (10 ml) was heated under reflux for 18 hours then allowed to cool to ambient temperature. The solvents were removed in vacuo and the residue was dried by azeotropic distillation with ethanol (50 ml) followed by ethyl acetate (50 ml). The solid remaining after removal of residual solvent in vacuo was crystallised from ethanol. The resulting product was collected by filtration, washed with ethanol (10 ml) and dried in vacuo at 60° C. to give 2-benzyl-3-[1-(4-chlorophenyl)cyclobutyl]-5,6-dihydroimidazo[2,1-b]-thiazole hydrobromide as white microneedles (2 g), m.p. 255-257° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06187802B1
Source datasetuspto-grants-2001_02
ORD IDord-db118e09af9f4a7da8b935c919aed534
Source noteuspto-grants-2001_02