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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795860Generated: November 4, 2026

Potassium Carbonate → HCID 22180671, compound

https://huagongshe.com/reaction/1795860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Aminopyrazin-1-ium iodideHCID 22180660—
ReactantHCID 22180661HCID 22180661—
SolventDimethylformamideHCID 6228—
ProductHCID 22180671HCID 2218067153.4%

Reaction Steps

To a mixture of 5-(phenylethynyl)-2-(phenylsulfonyl)pyridine (6.00 g) and K2CO3 (13.0 g) in DMF (120 mL) was added 1-aminopyrazin-1-ium iodide (12.6 g) and the mixture was stirred at room temperature for 1 h, then stirred at 60° C. for 8 h. To the reaction mixture was added K2CO3 (7.80 g) and 1-aminopyrazin-1-ium iodide (8.38 g) and stirred at room temperature for 1 h, then stirred at 60° C. for 12 h. To the reaction mixture was added further K2CO3 (7.80 g) and 1-aminopyrazin-1-ium iodide (8.38 g) and stirred at room temperature for 1 h, then stirred at 60° C. for 26 h. The mixture was poured into ice water and extracted with EtOAc, washed with water and brine, dried over sodium sulfate, evaporated in vacuo. The residue was purified by silica gel column chromatography (n-hexane-EtOAc 3:1 to CHCl3-MeOH 20:1) to give 2-phenyl-3-[6-(phenylsulfonyl)-3-pyridinyl]pyrazolo[1,5-a]pyrazine (4.14 g) as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030121B2
Source datasetuspto-grants-2006_04
ORD IDord-f7ce26d48007487f902b130deb9d7092
Source noteuspto-grants-2006_04