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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863936Generated: November 1, 2026

Hydrazine hydrate (1:1) → HCID 57973794, compound

https://huagongshe.com/reaction/1863936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 86614846HCID 86614846—
SolventEthanolHCID 702—
ProductHCID 57973794HCID 57973794—

Reaction Steps

A solution of 400 mg (1.15 mmol) of 5-bromo-2-(trifluoromethyl) [1,2,4]triazolo[1,5-a]pyrazine hydrobromide in 2.5 mL of dry ethanol was treated dropwise with 0.799 mL (11.5 mmol) of hydrazine hydrate, and stirring was continued at ambient temperature overnight. The reaction mixture was concentrated to dryness, and the residue was extracted with dichloromethane and then with tetrahydrofuran. The organic extracts were washed with saturated sodium bicarbonate aqueous solution, filtered, and concentrated. Purification of the residue by preparative HPLC (C18 reverse phase column, 10-60% acetonitrile in water containing 0.05% trifluoroacetic acid) afforded the title compound as a yellow solid. LC-MS 219 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625888B2
Source datasetuspto-grants-2009_12
ORD IDord-78adfffd80084326bb4f93ece1b66227
Source noteuspto-grants-2009_12