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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749674Generated: October 31, 2026

Hydrazine hydrate (1:1) → N',5-diamino-6-(5-tert-butyl-1,3,4-oxadiazol-2-yl)pyrazine-2-carboximidamide

https://huagongshe.com/reaction/1749674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant5-Amino-6-(5-tert-butyl-1,3,4-oxadiazol-2-yl)pyrazine-2-carbonitrileHCID 86727660—
SolventIsopropanolHCID 3776—
ProductN',5-diamino-6-(5-tert-butyl-1,3,4-oxadiazol-2-yl)pyrazine-2-carboximidamideHCID 9028326279.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

Hydrazine hydrate (82 mL, 1.69 mol) was added to 5-amino-6-(5-tert-butyl-1,3,4-oxadiazol-2-yl)pyrazine-2-carbonitrile (55 g, 225.18 mmol) in IPA (200 mL) and the mixture was heated at 50° C. under nitrogen for 16 hours. The mixture was cooled in an ice bath. The resulting precipitate was collected by filtration, washed with IPA and diethyl ether and dried to a constant weight to afford (Z)-5-amino-6-(5-tert-butyl-1,3,4-oxadiazol-2-yl)pyrazine-2-carbohydrazonamide (49.2 g, 79%) as a yellow solid: 1H NMR Spectrum: (DMSO-d6) 1.45 (9H, s), 5.26 (2H, s), 5.58 (2H, s), 7.56 (2H, s), 8.75 (1H, s); Mass Spectrum [M+H]+=277.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156831B2
Source datasetuspto-grants-2015_10
ORD IDord-f11d04d740a1410ca854735233997be9
Source noteuspto-grants-2015_10