HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795860Generated: November 4, 2026
Potassium Carbonate → HCID 22180671, compound
https://huagongshe.com/reaction/1795860
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Aminopyrazin-1-ium iodide | HCID 22180660 | — |
| Reactant | HCID 22180661 | HCID 22180661 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22180671 | HCID 22180671 | 53.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07030121B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-f7ce26d48007487f902b130deb9d7092 |
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| Source note | uspto-grants-2006_04 |
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