HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405309Generated: October 25, 2026
Water → (S)-2-(4-fluorophenyl)-3-(2-methylpyrrolidin-1-yl)-6-(2H-tetrazol-5-yl)quinoxaline
https://huagongshe.com/reaction/1405309
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | (S)-2-(4-Fluorophenyl)-3-(2-methylpyrrolidin-1-yl)quinoxaline-6-carbonitrile | HCID 70654208 | — |
| Reactant | HCID 178514644 | HCID 178514644 | — |
| Catalyst | Zinc bromide (ZnBr2); Zinc Dibromide | HCID 24375 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (S)-2-(4-fluorophenyl)-3-(2-methylpyrrolidin-1-yl)-6-(2H-tetrazol-5-yl)quinoxaline | HCID 60171473 | 63% |
Reaction Steps
To a solution of (S)-2-(4-fluorophenyl)-3-(2-methylpyrrolidin-1-yl)quinoxaline-6-carbonitrile (100 mg, 0.30 mmol) in DMSO (10 mL) was added dibromozinc (33.8 mg, 0.15 mmol), water (10 mL), azidosodium (48.8 mg, 0.75 mmol) and water (5 mL). The resulting solution was stirred for 1 days at 125° C. and then quenched by the addition of water (100 mL), extracted with dichloromethane (3×30 mL). The organic layers were combined and dried over anhydrous sodium sulfate and concentrated in vacuo to give a residue, which was purified via silica gel column chromatography (2% dichloromethane in methanol) to afford (S)-2-(4-fluorophenyl)-3-(2-methylpyrrolidin-1-yl)-6-(2H-tetrazol-5-yl)quinoxaline as a yellow solid (70.9 mg, 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916561B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-c9bee96bffa14a1fb7fe9c4edfb7a55f |
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| Source note | uspto-grants-2014_12 |
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