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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45862Generated: October 23, 2026

Gamma-Butyrolactone → HCID 178520695, compound

https://huagongshe.com/en/reaction/45862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGamma-ButyrolactoneHCID 7302—
ReactantSodium hexamethyidisilazaneHCID 45051731—
ReactantHCID 178507322HCID 178507322—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178520695HCID 17852069559%

Reaction Conditions

Temperature0 °C

Reaction Steps

30 mg (0.068 mmol) of 1-{3-[4-(2-aminopyridin-4-yl)-1H-pyrazol-3-yl]phenyl}-3-[4-(trifluoromethyl)phenyl]urea were dissolved in 2 ml of dry tetrahydrofuran and 15 μl (0.34 mmol) of γ-butyrolactone were added. The reaction mixture was cooled to 0° C. and a solution of 680 μl (0.68 mmol) of hexamethyldisilazane sodium salt 1M in THF in 2 ml of the same solvent were added dropwise. The mixture was maintained at 0° C. for 6 hours and at room temperature overnight, then partitioned between dichloromethane and water. The organic phase was dried over sodium sulphate and evaporated. The crude was finally purified by preparative HPLC in reverse phase conditions (basic eluant), giving 20 mg (59%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541575B2
Source datasetuspto-grants-2013_09
ORD IDord-3cff4afe910941b08835c59a82d566ad
Source noteuspto-grants-2013_09