HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043654Generated: November 4, 2026
tert-Butyl hydroperoxide → HCID 25235265, compound
https://huagongshe.com/reaction/1043654
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | HCID 86762101 | HCID 86762101 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 25235265 | HCID 25235265 | 29% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563550B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-ba675581e3fc416bab695ae3e54e89f4 |
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| Source note | uspto-grants-2013_10 |
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