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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717225Generated: October 31, 2026

Thiosemicarbazide → 5-(2,2,3,3-Tetrafluoro-1-methylcyclobutyl)-1,3,4-thiadiazol-2-amine

https://huagongshe.com/reaction/717225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiosemicarbazideHCID 2723789—
Reactant2,2,3,3-Tetrafluoro-1-(methyl)cyclobutanecarbonyl chlorideHCID 53398990—
Solvent1,4-DioxaneHCID 31275—
Product5-(2,2,3,3-Tetrafluoro-1-methylcyclobutyl)-1,3,4-thiadiazol-2-amineHCID 86629849—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 2,2,3,3-tetrafluoro-1-methylcyclobutanecarbonyl chloride (ABCR) (2 g, 9.78 mmol) and thiosemicarbazide (Aldrich) (0.891 g, 9.78 mmol) in 10 mL of dioxane was heated at 90° C. for 12 h. The solvent was evaporated under reduced pressure. The residue was dissolved in dichloromethane and washed with saturated NaHCO3. The organic extract was dried over Na2SO4 and concentrated. The residue was purified by flash chromatography on SiO2 (2% methanol in dichloromethane) to give the title compound. MS (ESI+) m/z 242 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193713B2
Source datasetuspto-grants-2015_11
ORD IDord-cec3a18d108d4608890470a4b1e454e7
Source noteuspto-grants-2015_11