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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1524459Generated: November 4, 2026

Ethanol → HCID 58045983, compound

https://huagongshe.com/reaction/1524459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 58045773HCID 58045773—
ProductHCID 58045983HCID 58045983—
ProductHCID 58046032HCID 58046032—

Reaction Conditions

Temperature50 °C

Reaction Steps

6-Chloro-8-trifluoromethyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine (W2.004; 65 mg) was initially charged in ethanol (6 ml) and admixed with sodium ethoxide (21 mg). The reaction mixture was stirred at 50° C. for 4 h. After cooling, the mixture was admixed with water and concentrated. The residue was taken up in ethyl acetate and washed with water three times. The ethyl acetate phase was dried over sodium sulfate, filtered and concentrated. The crude product was purified by means of preparative HPLC (met. E). The product-containing fractions, each of them clean, were combined, freed of the acetonitrile, adjusted to pH 9 with sodium hydrogencarbonate and extracted three times with ethyl acetate. The combined organic extracts were dried over sodium carbonate, filtered and concentrated. 15 mg of 6-ethoxy-8-trifluoromethyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine and 23 mg of 6-ethoxy-8-(ethoxydifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079906B2
Source datasetuspto-grants-2015_07
ORD IDord-f89f923417654d7daf430cbda8c68823
Source noteuspto-grants-2015_07