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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729864Generated: November 1, 2026

Dimethylformamide → 3-(1-METHYL-5-NITRO-2-IMIDAZOLYL)-6-FORMYLAMINO-S-TRIAZOLO [4,3-b]PYRIDAZINE

https://huagongshe.com/reaction/1729864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAcetic AnhydrideHCID 7918—
Reactant3-(5-Nitro-1-methyl-2-imidazolyl)-6-amino-s-triazolo[4,3-b]pyridazineHCID 21455924—
SolventFormic AcidHCID 284—
Product3-(1-METHYL-5-NITRO-2-IMIDAZOLYL)-6-FORMYLAMINO-S-TRIAZOLO [4,3-b]PYRIDAZINEHCID 21456004—

Reaction Steps

100 mg. 3-(5-nitro-1-methyl-2-imidazolyl)-6-amino-s-triazolo [4,3-b]pyridazine were suspended in 1.3 ml. dimethyl formamide and, after the addition of 1.5 ml. of the mixed anhydride obtainable from formic acid and acetic anhydride, stirred at ambient temperature until no more starting material could be detected by thin layer chromatography. The almost clear solution thus obtained was, after filtration, evaporated in a vacuum and the residue brought to crystallization with ether. There were thus obtained 72 mg. (65 percent of theory) 3-(1-methyl-5-nitro-2-imidazolyl)-6-formylamino-s-triazolo[4,3-b]pyridazine in the form of yellowish crystals which melt, with decomposition, at 200° - 204° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03989832
Source datasetuspto-grants-1976_11
ORD IDord-695898540b1347618a12eb1d229d7f9c
Source noteuspto-grants-1976_11