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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067605Generated: October 26, 2026

Water → Isopropyl 6-chloro[1,2,4]triazolo[1,5-b]pyridazine-2-carboxylate

https://huagongshe.com/reaction/1067605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsopropyl iodideHCID 6362—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Chloro-[1,2,4]triazolo[1,5-b]pyridazine-2-carboxylic acidHCID 22989292—
SolventDimethylformamideHCID 6228—
ProductIsopropyl 6-chloro[1,2,4]triazolo[1,5-b]pyridazine-2-carboxylateHCID 22989245—

Reaction Conditions

Temperature50 °C

Reaction Steps

2.14 g of 6-chloro[1,2,4]triazolo[1,5-b]pyridazine-2-carboxylic acid and 5.57 ml of N-ethyldiisopropylamine were dissolved in 30 ml of N,N-dimethylformamide; 3.23 ml of isopropyl iodide was added, followed by stirring at room temperature for 10 hours and at 50° C. for 3 hours. After cooling, water was added, followed by extraction with ethyl acetate; the extract was washed with saturated saline and dried with magnesium sulfate. The dry product was concentrated under reduced pressure; the residue was subjected to silica gel column chromatography and eluted with ethyl acetate. The desired fraction was collected and concentrated under reduced pressure to yield 2.21 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248740B1
Source datasetuspto-grants-2001_06
ORD IDord-3658b14e961f444c9585efa4a9a0fe50
Source noteuspto-grants-2001_06