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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272035Generated: November 2, 2026

2-Nitrophenol → HCID 10133802, compound

https://huagongshe.com/reaction/1272035

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitrophenolHCID 6947—
ReactantDiisopropylcarbodiimideHCID 12734—
Reactant3-(3-Fluoro-4-methoxybenzoyl)propionic acidHCID 67671—
Reactant1-(4-Pyridyl)piperazineHCID 70517—
SolventDimethylformamideHCID 6228—
Solvent1,2-DichloropropaneHCID 6564—
SolventTriethylamineHCID 8471—
ProductHCID 10133802HCID 10133802718.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208497B2
Source datasetuspto-grants-2007_04
ORD IDord-1f5f074e7d7d47c2a3273200454902ae
Source noteuspto-grants-2007_04