Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Nitrophenol | HCID 6947 | — |
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | 3-(3-Fluoro-4-methoxybenzoyl)propionic acid | HCID 67671 | — |
| Reactant | 1-(4-Pyridyl)piperazine | HCID 70517 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | 1,2-Dichloropropane | HCID 6564 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 10133802 | HCID 10133802 | 718.3% |
Reaction Steps
To the polymeric nitrophenol (1.5 g, approx. 1 mmol) was added a solution of 3-(4-methoxy-3-fluorobenzoyl)propionic acid (1.66 g, 7.34 mmol) in a mixture of 1,2-dichloropropane (15 ml) and DMF (6 ml), followed by the addition of DIC (0.78 ml, 5.01 mmol). The mixture was shaken at room temperature for 13 hours, filtered, and the polymer was extensively washed with DCM, DMF, and 1,2-dichloropropane. To the polymer was added 1,2-dichloropropane (5 ml), a solution of 1-(4-pyridyl)piperazine (116 mg, 0.71 mmol) in 1,2-dichloropropane (10 ml), and triethylamine (0.2 ml). The resulting mixture was shaken at room temperature for 21 hours, filtered, and the polymer was carefully washed with DCM and methanol. The combined filtrates were concentrated to yield the crude product as an oil (0.38 g). Crystallization from acetonitrile (2 ml) at −20° C. yielded 0.19 g (5.1 mmol, 72%) of the title compound as almost colourless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07208497B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-1f5f074e7d7d47c2a3273200454902ae |
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| Source note | uspto-grants-2007_04 |
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