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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9164Generated: October 25, 2026

1-Methylpiperazine → N-(6-Bromo-1,3-benzothiazol-2-yl)-N'-[4-(4-methylpiperazino)-4-oxobutyl]urea

https://huagongshe.com/reaction/9164

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantEthyl 4-([(6-bromo-1,3-benzothiazol-2-yl)amino]carbonylamino)butanoateHCID 21985597—
SolventTetrahydrofuranHCID 8028—
ProductN-(6-Bromo-1,3-benzothiazol-2-yl)-N'-[4-(4-methylpiperazino)-4-oxobutyl]ureaHCID 2198559058.7%

Reaction Steps

Ethyl 4-([(6-bromo-1,3-benzothiazol-2-yl)amino]carbonylamino)butanoate (100 mg, 0.259 mmol) was heated neat at about 80° C. in N-methyl-piperazine (259 mg, 2.59 mmol) for about 8 hrs. To the crude reaction mixture was added THF (2 mL), the ppt was filtered off and washed with THF (1 mL). The product was dried in vacuo and gave 67 mg (53%) pure product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091227B2
Source datasetuspto-grants-2006_08
ORD IDord-a7c760657744469984c092df1b5dee3f
Source noteuspto-grants-2006_08