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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237156Generated: October 31, 2026

Diisopropylethylamine → N-(4-Fluorophenyl)-N-(4-(pyridin-4-yloxy)phenyl)malonamide

https://huagongshe.com/reaction/2237156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant3-(4-Fluorophenylamino)-3-oxopropanoic acidHCID 4341843—
Reactant4-(Pyridin-4-yloxy)anilineHCID 11564589—
SolventDimethylformamideHCID 6228—
ProductN-(4-Fluorophenyl)-N-(4-(pyridin-4-yloxy)phenyl)malonamideHCID 1161027876.6%

Reaction Steps

A solution of 4-(4-aminophenoxy)pyridine (93 mg, 0.50 mmol) in DMF was treated with 3-(4-fluorophenylamino)-3-oxopropanoic acid (99 mg, 0.50 mmol), DIPEA (113 μL, 0.65 mmol) and TBTU (209 mg, 0.65 mmol) and the mixture was stirred at RT for 2 h. The mixture was concentrated to remove the DMF and the residue partitioned between EtOAc and saturated sodium bicarbonate solution. The EtOAc phase was washed with saturated sodium bicarbonate solution, brine, dried (MgSO4) and concentrated to give the title compound as an off-white foam (140 mg, 76%). 1H NMR (DMSO-d6) δ 10.30 (s, 1H), 10.24 (s, 1H), 8.43 (dd, 2H, J=5.5, 1.5 Hz), 7.70 (d, 2H, J=9.1 Hz), 7.63-7.60 (m, 2H), 7.17-7.14 (m, 4H), 6.89 (dd, 2H, J=5.5, 1.5 Hz), 3.46 (s, 2H); MS(ESI+) m/z 365.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714138B2
Source datasetuspto-grants-2010_05
ORD IDord-1c7916a233d844dbb11cdc418eeb08fa
Source noteuspto-grants-2010_05