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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921634Generated: October 26, 2026

N-bromobutanimide → 7-Bromo-2,4-bis(methylthio)imidazo[2,1-f][1,2,4]triazine

https://huagongshe.com/reaction/921634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2,4-Bis(methylthio)imidazo[2,1-f][1,2,4]triazineHCID 10680057—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product7-Bromo-2,4-bis(methylthio)imidazo[2,1-f][1,2,4]triazineHCID 5745764463.8%

Reaction Steps

A mixture of 2,4-bis(methylthio)imidazo[2,1-f][1,2,4]triazine (5.27 g, 24.82 mmol) and 1-bromopyrrolidine-2,5-dione (6.19 g, 34.8 mmol) in DMF (15 mL) was stirred at room temperature for 2 hours. The reaction was diluted with water, and the product extracted with dichloromethane (3×50 mL). The organic layer was washed with brine, dried and concentrated. The crude product mixture was purified via ISCO (0-50% of ethyl acetate/dichloromethane in 10 minutes, 80 g silica column) to give the pure product 7-bromo-2,4-bis(methylthio)imidazo[2,1-f][1,2,4]triazine (4.61 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273057B2
Source datasetuspto-grants-2016_03
ORD IDord-d3bb1f8412c746e7b3415af793a90b55
Source noteuspto-grants-2016_03