Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | Azd 3514 | HCID 46893585 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | AZD-3514 maleate | HCID 68496044 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258140B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-c5fb266b706040a68f0099a73fca1c58 |
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| Source note | uspto-grants-2012_09 |
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