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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204816Generated: October 26, 2026

Triphenylphosphine dibromide → 5-Bromo-3-(5-phenyl-1,3,4-thiadiazol-2-yl)pyrazin-2-amine

https://huagongshe.com/reaction/2204816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphine dibromideHCID 70579—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-aminobenzenecarbothioamideHCID 3361911—
Reactant3-Amino-6-bromopyrazine-2-carboxylic acidHCID 18521600—
SolventAcetonitrileHCID 6342—
Product5-Bromo-3-(5-phenyl-1,3,4-thiadiazol-2-yl)pyrazin-2-amineHCID 5947189143%

Reaction Steps

3-amino-6-bromo-pyrazine-2-carboxylic acid (1.000 g, 4.588 mmol) and benzenecarbothiohydrazide (759.1 mg, 4.588 mmol) were suspended in acetonitrile (25.00 mL), cooled in an ice bath and then treated with dibromo-triphenyl-phosphorane (4.453 g, 10.55 mmol) The reaction mixture was allowed to stir in an ice bath for 2 hours and then DIPEA (1.778 g, 2.396 mL, 13.76 mmol) was added slowly at 10° C. The reaction was left to stir at 0-10° C. for a further hour and the resultant precipitate was isolated by filtration, washed with a small amount of acetonitrile and dried (659 mg, 43% Yield). MS (ES+) 335.93

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365557B2
Source datasetuspto-grants-2016_06
ORD IDord-bb27ffc562fb4c958119190808e35673
Source noteuspto-grants-2016_06