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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522693Generated: October 28, 2026

Sulfoxonium, trimethyl-, iodide (1:1) → Tert-butyl 4-(5-(1-phenylcyclopropyl)pyrimidin-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/522693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
ReactantTert-butyl 4-(5-(1-phenylvinyl)pyrimidin-2-yl)piperazine-1-carboxylateHCID 118022644—
SolventDimethyl SulfoxideHCID 679—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(5-(1-phenylcyclopropyl)pyrimidin-2-yl)piperazine-1-carboxylateHCID 11802338510.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of tert-butyl 4-(5-(1-phenylvinyl)pyrimidin-2-yl)piperazine-1-carboxylate (366 mg, 1.0 mmol) in THF (20 mL) was added trimethylsulfoxonium iodide (1.1 g 5.0 mmol) in dimethyl sulfoxide (7 mL). The reaction mixture was stirred at 80° C. for 4 days, and diluted with ethyl acetate (200 mL). The organic phase was washed with water (200 mL) and brine (100 mL), dried over sodium sulfate, and concentrated. The residue was purified by silica gel chromatography (petroleum ether:ethyl acetate=20:1) to give tert-butyl 4-(5-(1-phenylcyclopropyl)pyrimidin-2-yl)piperazine-1-carboxylate (40 mg, 10%) as a yellow solid. MS (ES+) C22H28N4O2 requires: 380, found: 381 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334263B2
Source datasetuspto-grants-2016_05
ORD IDord-05b0bdd290d942239bcea83c4f5ab51d
Source noteuspto-grants-2016_05