HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209223Generated: November 4, 2026
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 4-Benzyloxy-6-chloro-pyrazolo[1,5-a]pyrazine-3-carbonitrile
https://huagongshe.com/reaction/2209223
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Amino-3-(benzyloxy)-5-chloropyrazin-1-ium 2,4,6-trimethylbenzenesulfonate | HCID 117843543 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-Benzyloxy-6-chloro-pyrazolo[1,5-a]pyrazine-3-carbonitrile | HCID 117843828 | — |
Reaction Steps
1-amino-3-(benzyloxy)-5-chloropyrazin-1-ium 2,4,6-trimethylbenzenesulfonate (5.34) (657 mg, 1.51 mmol) was suspended in 1,4-dioxane (5.75 mL) and acrylonitrile (0.23 mL, 3.5 mmol) was added followed by iPr2NEt (0.32 mL, 1.9 mmol). The resulting mixture was stirred for 1.75 h at r.t. and DDQ (720 mg, 3.2 mmol) was added in one portion. The resulting mixture was stirred an additional 1 h and was then partitioned between EtOAc, water and brine. The phases were separated and the aqueous phase was extracted with EtOAc. The combined organic phase was dried over Na2SO4, filtered, and concentrated. The concentrate was purified by silica gel chromatography (0-20% EtOAc in hexanes) to provide 4-(benzyloxy)-6-chloropyrazolo[1,5-a]pyrazine-3-carbonitrile. 1H NMR (400 MHz, Chloroform-d) δ 8.22 (s, 1H), 8.18 (s, 1H), 7.61-7.55 (m, 2H), 7.45-7.39 (m, 2H), 7.39-7.33 (m, 1H), 5.67 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376441B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-c76b946a745d4aefb848ad6a3ef96089 |
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| Source note | uspto-grants-2016_06 |
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