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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415894Generated: October 29, 2026

Phthalimide → HCID 11963016, compound

https://huagongshe.com/reaction/415894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 59598421HCID 59598421—
SolventDichloromethaneHCID 6344—
ProductHCID 11963016HCID 1196301688%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088794B2
Source datasetuspto-grants-2012_01
ORD IDord-3011202b9e5c4b98933681ccca3221e7
Source noteuspto-grants-2012_01