HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535708Generated: October 28, 2026
Water → 5-Bromo-8-(4-methylpiperazin-1-yl)tetrazolo[1,5-a]pyrazine
https://huagongshe.com/reaction/535708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 8-(4-Methylpiperazin-1-yl)tetrazolo[1,5-a]pyrazine | HCID 86696146 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-Bromo-8-(4-methylpiperazin-1-yl)tetrazolo[1,5-a]pyrazine | HCID 86696147 | 100% |
Reaction Steps
8-(4-Methylpiperazin-1-yl)tetrazolo[1,5-a]pyrazine (100 g, 0.456 mol, 1.0 eq.) was suspended in acetic acid (110 ml) under nitrogen and stirred at 35° C. until a solution was obtained. The solution was cooled to 16° C. and N-Bromosuccinimide (82.14 g, 0.461 mol, 1.01 eq.) is added at such a rate that the temperature of the reaction was maintained at 14-18° C. The reaction was monitored and additional aliquots of N-bromosuccinimide added as necessary to ensure conversion was ≧99.5% after 2-3 hours stirring at 20° C. stirring. Water was added, and the solution is cooled to 13° C. The pH of the suspension is adjusted to 8.3-8.5 by addition of triethylamine. The resulting suspension was filtered, washed with water, and dried to afford the desired product (136.02 g, 100% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859550B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-8350dc92155848e1a3bc2244bafb2b62 |
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| Source note | uspto-grants-2014_10 |
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