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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729871Generated: November 1, 2026

1-Methylpiperazine → HCID 21455926, compound

https://huagongshe.com/reaction/1729871

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 21455917HCID 21455917—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 21455926HCID 21455926—

Reaction Steps

In a manner analogous to that described in Example 21, 4.22 g. crude 3-(5-nitro-1-β-acetoxyethyl-2-imidazolyl)-6-chloro-s-triazolo[4,3-b]pyridazine were reacted with 4 g. 4-methylpiperazine in 20 ml. dioxan; after evaporation of the reaction mixture, the residue remaining behind was repeatedly digested with petroleum ether and then recrystallized from 15 ml. isopropanol, left to stand overnight and the crystals then filtered off with suction and washed with water. There were thus obtained 2.4 g. 3-(5-nitro- 1-β-acetoxyethyl-2-imidazolyl)-6-(4-methyl-1-piperazinyl)-s-triazolo[4,3-b]pyridazine, which has a melting point of 168° - 170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03989832
Source datasetuspto-grants-1976_11
ORD IDord-049c4638c07246e88db35f64445862ad
Source noteuspto-grants-1976_11