Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051422Generated: October 31, 2026

N-bromobutanimide → N-(5-bromothiazol-4-yl)acetamide

https://huagongshe.com/reaction/1051422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-AcetamidothiazoleHCID 20294037—
SolventAcetic acid tetrahydrofuranHCID 23444217—
ProductN-(5-bromothiazol-4-yl)acetamideHCID 8671555654.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

1-Bromopyrrolidine-2,5-dione (0.48 g, 2.67 mmol) was added to the solution of N-(thiazol-4-yl)acetamide (0.38 g, 2.67 mmol) in AcOH/THF (10 mL/10 mL). The mixture was heated to 25° C. for 2 h. The solvent was removed and the solution was adjusted to pH˜9 with 2 N NaOH solution. It was extracted with EA (3×50 mL), the combined organic phase was washed with brine, dried with Na2SO4 and concentrated to give the title compound (1.32 g, 1.45 mmol, 54.2%) as light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388180B2
Source datasetuspto-grants-2016_07
ORD IDord-b6376ab244d74ea6a62023c32bb595e4
Source noteuspto-grants-2016_07