Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492708Generated: October 30, 2026

Dimethylformamide → HCID 23153052, compound

https://huagongshe.com/reaction/492708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantHCID 23153189HCID 23153189—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
SolventEthylacetate methanolHCID 21584119—
ProductHCID 23153052HCID 2315305257.5%

Reaction Steps

To a solution of 4-(4-amino-3-methylphenoxy)pyridin-2-ylamine (765 mg, 3.55 mmol) in N,N-dimethylformamide (15.0 ml) were added N-(4-fluorophenyl)malonic acid (770 mg, 3.91 mmol), triethylamine (0.544 ml, 3.91 mmol) and benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (1.73 g, 3.91 mmol), followed by stirring at room temperature for 13 hrs. The reaction mixture was partitioned between ethyl acetate (200 ml) and a saturated aqueous solution of sodium hydrogencarbonate (80 ml). The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate. The solvent was evaporated to give a residue, which was then subjected to silica gel column chromatography (ethyl acetate, then ethyl acetate/methanol=20/1 to 10/1). To the resultant crude product were added ethanol (0.5 ml) and diethyl ether (10 ml) to suspend. A solid was filtered off, washed with diethyl ether, and dried under aeration to provide the titled compound (805 mg, 57.5%) as pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531532B2
Source datasetuspto-grants-2009_05
ORD IDord-b1a71939d29248e2b059aa9178e5594d
Source noteuspto-grants-2009_05