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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447165Generated: November 3, 2026

Ethanol → HCID 20551574, compound

https://huagongshe.com/reaction/1447165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 20551567HCID 20551567—
SolventWaterHCID 962—
ProductHCID 20551574HCID 2055157470%

Reaction Steps

A mixture of 12.0 g (0.048 mole) of 1-bromo-s-triazolo[3,4-c]benzo-as-triazine, 40 ml of N-methyl-piperazine and 80 ml of ethanol is refluxed for 2 hours. The solution is poured into water and the product is extracted mit methylene chloride. The solvent is evaporated from the extract and the residue is recrystallized from benzene. 9.7 g (70%) of 1-(N-methyl-piperazino)-s-triazolo[3,4-c]benzo-as-triazine are obtained; m.p.: 162°-163° C. This product is added to a suspension of 12 g (0.068 moles) of sodium dithionite in 100 ml of water, and reduced into the respective dihydro compound under argon atmosphere. The separated precipitate is filtered off, dried, admixed with 50 ml of propionic anhydride, and the mixture is heated at 120° to 125° C. for 2 hours. The reaction mixture is cooled and the separated product is filtered off. 12.3 g (67.0%) of the title compound are obtained; m.p.: 173°-175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04316022
Source datasetuspto-grants-1982_02
ORD IDord-20c875a2d3de4bb4978a9acb41cbbf73
Source noteuspto-grants-1982_02