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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657850Generated: October 30, 2026

Water → 6-Cyclopropylmethoxy-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine

https://huagongshe.com/reaction/657850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantCyclopropanemethanolHCID 75644—
Reactant6-Chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine hydrobromideHCID 86650794—
SolventDimethylformamideHCID 6228—
Product6-Cyclopropylmethoxy-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamineHCID 58136964—

Reaction Conditions

Temperature40 °C

Reaction Steps

Cyclopropylmethanol (2.64 ml) was initially charged in DMF (35 ml), admixed under argon with sodium hydride (795 mg) and stirred at 40° C. for 1 h. Subsequently, 6-chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine hydrobromide (W2.001; 1.66 g), dissolved in DMF (35 ml), were added dropwise. After 1 h, the mixture was admixed with water and extracted by shaking four times with dichloromethane. The combined organic phases were dried over magnesium sulfate and concentrated by rotary evaporation. The residue was triturated with MtB ether, filtered off with suction and dried. 720 mg of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076336B2
Source datasetuspto-grants-2011_12
ORD IDord-da0f28ff919f4941a8028bc1e32a934a
Source noteuspto-grants-2011_12