Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 59598421 | HCID 59598421 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11963016 | HCID 11963016 | 88% |
Reaction Steps
To a solution of N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-1-(2-hydroxyethyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide (0.20 g, 0.38 mmol) and phthalimide (0.11 g, 0.76 mmol) in 10 mL of CH2Cl2 was added triphenyl phosphine (0.13 ml, 0.57 mmol), followed by diethyl azodicarboxylate (0.089 ml, 0.57 mmol) via a syringe. The reaction mixture was stirred at RT for 16 hours. The resulting solution was concentrated in vacuo, and the residue was purified by silica gel chromatography (EtOAc to 10% MeOH/EtOAc) to give the title compound as a light yellow solid (0.22 g, 88% yield). MS (ESI pos. ion) m/z: 658 (MH+). Calc'd exact mass for C37H28FN5O6: 657. 1H NMR (300 MHz, MeOH) 8.53 (1 H, d, J=5.5 Hz), 8.28 (1 H, d, J=9.0 Hz), 7.80-7.91 (5 H, m), 7.50 (1 H, s), 7.48 (2 H, d, J=3.0 Hz), 7.26-7.36 (6 H, m), 6.49 (1 H, dd, J=5.4, 1.0 Hz), 4.27 (2 H, t, J=5.5 Hz), 3.97 (3 H, s), 3.74 (2 H, t, J=5.5 Hz), 2.68 (3 H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088794B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-3011202b9e5c4b98933681ccca3221e7 |
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| Source note | uspto-grants-2012_01 |
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