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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783915Generated: October 30, 2026

Sodium Bicarbonate → 5,8-Dibromo-(1,2,4)triazolo(1,5-a)pyrazine

https://huagongshe.com/reaction/1783915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178526378HCID 178526378—
SolventWaterHCID 962—
Product5,8-Dibromo-(1,2,4)triazolo(1,5-a)pyrazineHCID 4975802262.1%

Reaction Steps

N-(3,6-dibromo-pyrazin-2-yl)-N′-hydroxyformamidine (17.4 mg, 58.80 mmol) is treated with polyphosphoric acid (150 g) for one hour at 50° C. and then for 1.75 hours at 70° C. After cooling to room temperature, water is added to the reaction mixture. The resultant suspension is brought to pH 8 by careful addition of solid NaHCO3 in small portions. The precipitate formed is collected by filtration, washed once with 1N NaOH, three times with water and dried in vacuo. The residue is partitioned between ethyl acetate and 1N NaOH and the organic phase is washed one more time with 1N NaOH and once with brine. The organic phase is dried over MgSO4, filtered and evaporated to give the title compound (10.15 g) as a white solid. 1H-NMR (400 MHz, d6-DMSO) δ(ppm) 8.43 (s, 1H), 8.92 (s, 1H). LCMS: Rt 2.73 min (94.2%), m/z (APCI) 277 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501411B2
Source datasetuspto-grants-2009_03
ORD IDord-8435ddd943c94774ab8a007e9038c22c
Source noteuspto-grants-2009_03