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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876854Generated: October 26, 2026

Hydrochloric Acid → (4-(4-(2-chloropyrimidin-4-yl)-1H-pyrazol-1-yl)-1-(cyclopropylsulfonyl)piperidin-4-yl)acetonitrile

https://huagongshe.com/reaction/1876854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantCyclopropanesulfonyl chlorideHCID 2760919—
Reactanttert-butyl 4-(4-(2-chloropyrimidin-4-yl)-1H-pyrazol-1-yl)-4-(cyanomethyl)piperidine-1-carboxylateHCID 86637283—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product(4-(4-(2-chloropyrimidin-4-yl)-1H-pyrazol-1-yl)-1-(cyclopropylsulfonyl)piperidin-4-yl)acetonitrileHCID 86637287—

Reaction Steps

To a mixture of tert-butyl 4-(4-(2-chloropyrimidin-4-yl)-1H-pyrazol-1-yl)-4-(cyanomethyl)piperidine-1-carboxylate (0.487 g, 1.21 mmol) in 2 mL of dioxane was added 4 M HCl in dioxane (4.0 mL). The reaction was stirred at room temperature for 30 min, then evaporated to dryness. To the resulting crude HCl salt in methylene chloride (9.4 mL) was added triethylamine (0.505 mL, 3.62 mmol) followed by cyclopropanesulfonyl chloride (0.148 mL, 1.45 mmol). The mixture was stirred at room temperature for 30 min, washed with saturated sodium bicarbonate, dried, and evaporated to dryness. The residue was used directly in next step (402 mg, 82%). LCMS (M+H) 407.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309718B2
Source datasetuspto-grants-2012_11
ORD IDord-4fff269e04d2425ab316c0d6a9f5568b
Source noteuspto-grants-2012_11