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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217671Generated: October 29, 2026

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

https://huagongshe.com/reaction/217671

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 numberUS08198272B2
Source datasetuspto-grants-2012_06
ORD IDord-5cb1cf8eccae46e48c9a52bb78ccc5b4
Source noteuspto-grants-2012_06