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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521247Generated: October 30, 2026

Methanesulfonyl chloride → HCID 86729424, compound

https://huagongshe.com/reaction/521247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium AzideHCID 33557—
ReactantHCID 86729423HCID 86729423—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductHCID 86729424HCID 86729424—

Reaction Steps

To a solution of 1-[1-(cyanomethyl)-4-hydroxycyclohexyl]-3-[(4-fluorophenyl)amino]-1H-pyrazole-4-carboxamide (75 mg, 0.21 mmol) in DCM (2 mL) at ambient temperature was added TEA (0.059 mL, 0.42 mmol), and methanesulfonyl chloride (0.020 mL, 0.25 mmol). The mixture was stirred at ambient temperature for 10 minutes. The mixture was diluted with saturated aqueous NaHCO3, and extracted with EtOAc. The organic layer was separated, washed with brine, dried over anhydrous MgSO4 and concentrated in vacuo. The crude residue (90 mg, 0.207 mmol) was diluted in DMF (1.0 mL), NaN3 (27 mg, 0.41 mmol) was added and the mixture was heated at 90° C. for 16 hours. The mixture was cooled to ambient temperature, diluted with H2O and extracted with EtOAc. The organic layer was separated, washed with brine, dried over anhydrous MgSO4 and concentrated in vacuo. The residue was purified by MPLC on silica gel (using a gradient elution of 30-100% EtOAc/hexanes) to give the title compound as a mixture of two diasteromers (ratio 1:3), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328099B2
Source datasetuspto-grants-2016_05
ORD IDord-3ad21a876b334e2ea1a60538c159003c
Source noteuspto-grants-2016_05