HuagongsheHuagongshe Chemistry Print Report · For research reference only
Maleic Acid → 1-(1-((6-Cyclopropyl-2,4'-difluoro-3-isopropoxybiphenyl-4-yl)methyl)piperidin-4-yl)-3-methyl-2-oxo-1,2-dihydropyridine-4-carboxylic acid maleate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | 1-(1-((6-Cyclopropyl-2,4'-difluoro-3-isopropoxybiphenyl-4-yl)methyl)piperidin-4-yl)-3-methyl-2-oxo-1,2-dihydropyridine-4-carboxylic acid | HCID 91754670 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(1-((6-Cyclopropyl-2,4'-difluoro-3-isopropoxybiphenyl-4-yl)methyl)piperidin-4-yl)-3-methyl-2-oxo-1,2-dihydropyridine-4-carboxylic acid maleate | HCID 118037600 | 91.8% |
Reaction Steps
Maleic acid (111 mg) was added to a solution of 1-(1-((6-cyclopropyl-2,4′-difluoro-3-isopropoxybiphenyl-4-yl)methyl)piperidin-4-yl)-3-methyl-2-oxo-1,2-dihydropyridine-4-carboxylic acid (513 mg) in ethanol (5 mL) at room temperature. The mixture was stirred at the same temperature under nitrogen atmosphere for 1 hour and concentrated in vacuo. The residue was crystallized from ethyl acetate-hexane to give a colorless solid. The solid was recrystallized from ethanol-heptane to give the title compound (573 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120777B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-11d3c1b54e584637aad48b9553be58ba |
| Source note | uspto-grants-2015_09 |