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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729866Generated: November 3, 2026

Methane → 3-(5-Nitro-1-methyl-2-imidazolyl)-6-acetamido-s-triazolo[4,3-b]pyridazine

https://huagongshe.com/reaction/1729866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantAcetic AnhydrideHCID 7918—
Reactant3-(5-Nitro-1-methyl-2-imidazolyl)-6-amino-s-triazolo[4,3-b]pyridazineHCID 21455924—
Product3-(5-Nitro-1-methyl-2-imidazolyl)-6-acetamido-s-triazolo[4,3-b]pyridazineHCID 21455972—

Reaction Steps

1.45 g. 3-(5-nitro-1-methyl-2-imidazolyl)-6-amino-s-triazolo [4,3-b]pyridazine was boiled under reflux with 22 ml. acetic anhydride for 1.5 hours at 160° C. bath temperature, the solution obtained was then mixed with charcoal, suction filtered while still hot, washed with a little acetic anhydride and then with ether and dried for 3 hours at 120° C. There was thus obtained 0.79 g. of the desired 3-(5-nitro-1-methyl-2-imidazolyl)-6-acetamido-s-triazolo [4,3-b]pyridazine in the form of yellow-white crystals which melt at 238° - 239° C. and show a change above 230° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03989832
Source datasetuspto-grants-1976_11
ORD IDord-01741fc6ceec4b92b546c682bf605185
Source noteuspto-grants-1976_11