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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247622Generated: November 1, 2026

Guanidine Hydrochloride → 3-Amino-1,2,4-benzotriazine

https://huagongshe.com/reaction/1247622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantNitrobenzeneHCID 7416—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
Product3-Amino-1,2,4-benzotriazineHCID 8833672%

Reaction Steps

To a stirring mixture of guanidine hydrochloride (160 mg, 1.7 mmol) and t-BuOK (670 mg, 6 mmol) in DMSO (4 mL) was added one portion of nitrobenzene (123 mg, 1 mmol) at room temperature. The mixture turned red in one minute. In 20 to 30 minutes the mixture was quenched with a saturated, aqueous solution of ammonium chloride. A yellow precipitate was formed and removed by filtration. The precipitate was then washed with water, dried in the air, and recrystallized from benzene or ethanol to give 105 mg (72%) of 3-amino-1,2,4-benzotriazine. The melting point was determined to be 203–205° C., consistent with the melting point (207° C.) of 3-amino-1,2,4-benzotriazine synthesized by other known methods (J. Chem. Soc. (B) (1970) 911).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129349B2
Source datasetuspto-grants-2006_10
ORD IDord-ee9818244242460289efada25e1f7a5e
Source noteuspto-grants-2006_10