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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043654Generated: November 4, 2026

tert-Butyl hydroperoxide → HCID 25235265, compound

https://huagongshe.com/reaction/1043654

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl hydroperoxideHCID 6410—
ReactantN-MethylbenzylamineHCID 7669—
ReactantHCID 86762101HCID 86762101—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 25235265HCID 2523526529%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Dimethylamino-imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde (116 mg, 0.591 mmol) was dissolved in dry acetonitrile (4 mL) and N-methylbenzylamine (0.768 mmol, 0.1 mL) and t-butylhydroperoxide (0.768 mmol, 5.5M, 0.14 mL) were added. The mixture was heated at 80° C. for 10 hours. The reaction mixture was diluted with water (4 mL) at room temperature and extracted with dichloromethane (3×8 mL). The combined organic layer was dried over sodium sulphate and concentrated in vacuo. The crude product was purified by flash chromatography (Isolute cartridge SiII, ethyl acetate:dichloromethane, 1:9 to 10:0) yielding 54 mg of 2-dimethylamino-imidazo[2,1-b][1,3,4]thiadiazole-5-carboxylic acid benzyl-methyl-amide as yellowish solid (29% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563550B2
Source datasetuspto-grants-2013_10
ORD IDord-ba675581e3fc416bab695ae3e54e89f4
Source noteuspto-grants-2013_10