Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747249Generated: October 30, 2026

Chlorosuccinimide → HCID 86665223, compound

https://huagongshe.com/reaction/1747249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantPotassium BicarbonateHCID 516893—
Reactanttert-butyl (4-ethenylphenyl)carbamateHCID 11736129—
Reactant2-(1-{[3,5-Bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazole-4-carbaldehyde oximeHCID 86665221—
CatalystWaterHCID 962—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 86665223HCID 86665223—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazole-4-carbaldehyde oxime (1.50 g) and tert-butyl (4-vinylphenyl)carbamate (0.94 g) in ethyl acetate (140 ml) were added, at room temperature, potassium hydrogencarbonate (1.79 g) and N-chlorosuccinimide (0.50 g), and then one drop of water. After the reaction mixture had been stirred at 60° C. for 3 h, ethyl acetate and water were added, and the mixture was extracted with ethyl acetate. The organic extracts were dried over sodium sulphate and concentrated under reduced pressure. The residue was purified by chromatography. This gave tert-butyl (4-{3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}phenyl)carbamate (0.90 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150565B2
Source datasetuspto-grants-2015_10
ORD IDord-ab8000e95b984378ae2d3bba60199efa
Source noteuspto-grants-2015_10