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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035784Generated: October 30, 2026

Water → HCID 67524617, compound

https://huagongshe.com/reaction/1035784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCyclohexanolHCID 7966—
ReactantSodium hydrideHCID 24758—
Reactant3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazineHCID 1482346—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67524617HCID 6752461727.5%

Reaction Steps

106 mg of sodium hydride at 60% in oil are added to a solution of 530 mg of cyclohexanol in 5 cm3 of tetrahydrofuran at 0° C. under argon. After stirring for 15 min, 500 mg of 3,6-dichloro[1,2,4]triazolo[4,3-b]pyridazine (commercial) are added. The brown suspension is stirred, allowing the temperature to return gradually to 20° C. for 24 h. The reaction medium is poured into water and the mixture is extracted with ethyl acetate. After concentration to dryness under vacuum, a brown powder is obtained, which is washed with ether. The filtrate is concentrated to dryness and the oily yellow residue is chromatographed on Biotage Quad 12/25 (KP-SIL, 60 Å; 32-63 μm), elution being carried out with a gradient of 100% dichloromethane to 95:5 dichloromethane/methanol. 184 mg of 3-chloro-6-(cyclohexyloxy)[1,2,4]triazolo[4,3-b]pyridazine are thus obtained in the form of a white powder, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546393B2
Source datasetuspto-grants-2013_10
ORD IDord-86e07a1b940b4c6bb4cdc077cee68293
Source noteuspto-grants-2013_10