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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1853142Generated: October 25, 2026

Triethylamine → 3-amino-6-bromo-N'-(phenylcarbonyl)pyrazine-2-carbohydrazide

https://huagongshe.com/reaction/1853142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzoylhydrazineHCID 11955—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant3-Amino-6-bromopyrazine-2-carboxylic acidHCID 18521600—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-amino-6-bromo-N'-(phenylcarbonyl)pyrazine-2-carbohydrazideHCID 5947235573.5%

Reaction Steps

TBTU (22.09 g, 68.80 mmol) and triethylamine (4.642 g, 6.394 mL, 45.87 mmol) were added to a suspension of 3-amino-6-bromo-pyrazine-2-carboxylic acid (10 g, 45.87 mmol) and benzohydrazide (7.494 g, 55.04 mmol) in DMF (100.0 mL) and the resulting solution stirred at ambient temperature for 48 hours and then poured into water (400 mL) with vigorous stirring. This was allowed to stir for 30 minutes, filtered and washed with water. The moist solid was dissolved in hot EtOAc, dried (MgSO4), filtered and concentrated in vacuo and the resultant solid dried under vacuum to give the desired product (11.34 g, 73% Yield). 1H NMR (400.0 MHz, DMSO) δ 7.51 (2H, m), 7.61 (1H, m), 7.69 (2H, br s), 7.92 (2H, m), 8.44 (1H, s), 10.48 (1H, br s), 10.54 (1H, br s) ppm; MS (ES+) 338.01.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962631B2
Source datasetuspto-grants-2015_02
ORD IDord-1b078a1358e44cd5b7d6c87a8efac7de
Source noteuspto-grants-2015_02