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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959420Generated: October 26, 2026

4-(Bromomethyl)benzoic acid → 5-Bromo-3-(5-(4-(bromomethyl)phenyl)-1,3,4-oxadiazol-2-yl)pyrazin-2-amine

https://huagongshe.com/reaction/1959420

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Bromomethyl)benzoic acidHCID 22599—
ReactantTriphenylphosphine dibromideHCID 70579—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Amino-6-bromopyrazine-2-carbohydrazideHCID 58070256—
SolventAcetonitrileHCID 6342—
Product5-Bromo-3-(5-(4-(bromomethyl)phenyl)-1,3,4-oxadiazol-2-yl)pyrazin-2-amineHCID 5807046768%

Reaction Steps

To a suspension of 3-amino-6-bromo-pyrazine-2-carbohydrazide (200 mg, 0.86 mmol) and 4-(bromomethyl)benzoic acid (185 mg, 0.86 mmol) in MeCN (4 mL) at room temperature was added dibromo(triphenyl)phosphorane (1.7 g, 4.14 mmol) and the resulting reaction mixture was stirred for 1 h. The reaction mixture was diluted with acetonitrile (2 mL) and DIPEA (668 mg, 900 μL, 5.2 mmol) was added dropwise and the suspension was allowed to stir overnight. The suspension was filtered, washed with CH3CN and hexane, and air dried to provide 5-bromo-3-(5-(4-(bromomethyl)phenyl)-1,3,4-oxadiazol-2-yl)pyrazin-2-amine (240 mg, 68%) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 8.45 (s, 1H), 8.11 (d, J=8.1 Hz, 2H), 7.72 (d, J=8.2 Hz, 2H), 4.82 (s, 2H). LC/MS m/z 412.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410112B2
Source datasetuspto-grants-2013_04
ORD IDord-7dbb65f850104a4fb3eb2cc391c7fe01
Source noteuspto-grants-2013_04