Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035762Generated: October 30, 2026

Water → 3-Chloro-6-(morpholin-4-yl)[1,2,4]triazolo[4,3-b]pyridazine

https://huagongshe.com/reaction/1035762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMorpholineHCID 8083—
ReactantTriethylamineHCID 8471—
Reactant3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazineHCID 1482346—
SolventDimethylformamideHCID 6228—
Product3-Chloro-6-(morpholin-4-yl)[1,2,4]triazolo[4,3-b]pyridazineHCID 21822190—

Reaction Conditions

Temperature20 °C

Reaction Steps

0.9 cm3 of morpholine and 1.4 cm3 of triethylamine are added to a solution of 1.89 g of commercial 3,6-dichloro[1,2,4]triazolo[4,3-b]pyridazine in 20 cm3 of N,N-dimethylformamide. The reaction is stirred at 20° C. for 19 h. 60 cm3 of water are added and the mixture is extracted with ethyl acetate. The organic phase is washed with water and with brine and then dried over magnesium sulphate and concentrated to dryness, to give a beige solid. The latter is chromatographed by solid deposit on a Merck cartridge of 70 g of silica 15-40 μm, elution being carried out with a gradient of 100% dichloromethane to 95/5 dichloromethane/methanol. 1.97 g of 3-chloro-6-(morpholin-4-yl)[1,2,4]triazolo[4,3-b]pyridazine are obtained in the form of a very pale yellow solid, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546393B2
Source datasetuspto-grants-2013_10
ORD IDord-76c41f627482447f90fa32355650c736
Source noteuspto-grants-2013_10