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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252871Generated: October 30, 2026

N-bromobutanimide → Methyl 2-(4-(4-cyanobenzyl)piperazin-1-yl)thiazole-5-carboxylate

https://huagongshe.com/reaction/252871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 3-methoxyacrylateHCID 5323651—
Reactant4-(4-Cyanobenzyl)piperazine-1-carbothioamideHCID 86040437—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
ProductMethyl 2-(4-(4-cyanobenzyl)piperazin-1-yl)thiazole-5-carboxylateHCID 6689423477.1%

Reaction Steps

A solution of (E)-methyl 3-methoxyacrylate (290 mg, 280 mL, 2.51 mmol) in 1:1 mixture of dioxane/water (4 mL) was treated with NBS (507 mg, 2.85 mmol) at 0° C. and stirred for 1 hour. The mixture was transferred to a flask containing the thioamide 337 (593 mg, 2.28 mmol) at room temperature and the resulting mixture was refluxed for 1.5 hours. It was cooled down, quenched by adding saturated NH4Cl solution (5 mL) and concentrated. Obtained material was partitioned between EtOAc and water. Organic phase was dried with Na2SO4, filtered and concentrated. The crude product was purified by flash chromatography using 60% EtOAc in hexanes as an eluent, to afford the title compound 338 (602 mg, 77% yield). MS: calc: 342.1; found: 343.1 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868205B2
Source datasetuspto-grants-2011_01
ORD IDord-3db03a48cd0b4b149dd3b720fbfaac38
Source noteuspto-grants-2011_01