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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantN-bromobutanimideHCID 67184—
Reactant8-(4-Methylpiperazin-1-yl)tetrazolo[1,5-a]pyrazineHCID 86696146—
SolventAcetic AcidHCID 176—
Product5-Bromo-8-(4-methylpiperazin-1-yl)tetrazolo[1,5-a]pyrazineHCID 86696147100%

Reaction Conditions

Temperature35 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859550B2
Source datasetuspto-grants-2014_10
ORD IDord-8350dc92155848e1a3bc2244bafb2b62
Source noteuspto-grants-2014_10