Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3-(5-formyl-2,4-dimethyl-1H-pyrrol-3-yl)propanoic Acid | HCID 1512520 | — |
| Reactant | HCID 9948092 | HCID 9948092 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69883661 | HCID 69883661 | 58.2% |
Reaction Steps
A mixture of 4-[2-(4-isopropyl-phenoxy)-ethyl]-1,3-dihydro-indol-2-one (118 mg, 0.4 mmol), 4-carboxyethyl-3,5-dimethyl-2-formylpyrrole (78 mg, 0.4 mmol) and piperidine (0.3 mL) in 1.0 mL of ethanol was heated in a sealed tube at 90° C. for 18 hours and cooled to room temperature. The reaction mixture was concentrated and the residue was dissolved in methylene chloride followed by the addition of diethyl ether. The precipitate was filtered and washed with ethyl acetate to give 110 mg (58%) of 3-(5-{4-[2-(4-isopropyl-phenoxy)-ethyl]-2-oxo-1,2-dihydro-indol-3-ylidenemethyl}-2,4-dimethyl-1H-pyrrol-3-yl)-propionic acid (piperidine salt).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06689806B1 |
|---|
| Source dataset | uspto-grants-2004_02 |
|---|
| ORD ID | ord-c4f95d54eb4f4d34aa7fd924648af937 |
|---|
| Source note | uspto-grants-2004_02 |
|---|