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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381106Generated: November 3, 2026

Ethyl Acetate → AZD-3514 maleate

https://huagongshe.com/reaction/2381106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantMaleic AcidHCID 444266—
ReactantAzd 3514HCID 46893585—
SolventMethanolHCID 887—
ProductAZD-3514 maleateHCID 6849604490%

Reaction Conditions

Temperature50 °C

Reaction Steps

is A clear solution of maleic acid (0.445 g, 3.84 m mol) in methanol (1.0 mL) was added to a clear solution of 6-(4-{4-[2-(4-acetylpiperazin-1-yl)ethoxy]phenyl}piperidin-1-yl)-3-(trifluoromethyl)-7,8-dihydro[1,2,4]triazolo[4,3-b]pyridazine, obtained as described in Example 5.5, (2.0 g, 3.84 m mol) in methanol (2.0 mL) at 22-25° C. and the resulting clear solution heated to 50° C. for 30 min. The reaction mass was cooled to 22-25° C. and ethylacetate (16.0 mL) added drop wise to the reaction mass at 22-25° C. The reaction mass was then stirred for 60 min at 22-25° C. The resulting white color material was collected by filtration and washed with ethylacetate (5.0 mL). The material was dried under reduced pressure with nitrogen gas bleed at 50° C. to afford the desired product 6-(4-{4-[2-(4-acetylpiperazin-1-yl)ethoxy]phenyl}piperidin-1-yl)-3-(trifluoromethyl)-7,8-dihydro[1,2,4]triazolo[4,3-b]pyridazine maleate (2.21 g, 90.0%) as free flowing white color material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258140B2
Source datasetuspto-grants-2012_09
ORD IDord-c5fb266b706040a68f0099a73fca1c58
Source noteuspto-grants-2012_09