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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499718Generated: October 30, 2026

Felbinac → HCID 10269797, compound

https://huagongshe.com/reaction/499718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFelbinacHCID 3332—
Reactant1,2-DichloropropaneHCID 6564—
Reactant2-NitrophenolHCID 6947—
ReactantDiisopropylcarbodiimideHCID 12734—
Reactant1-Methyl-4-(methylamino)piperidineHCID 566323—
SolventDimethylformamideHCID 6228—
ProductHCID 10269797HCID 1026979742%

Reaction Steps

To the polymeric nitrophenol (1.5 g, approx. 1 mmol) was added a filtered solution of 4-biphenylylacetic acid (1.10 g, 5.18 mmol) in a mixture of 1,2-dichloropropane (18 ml) and DMF (2 ml), followed by the addition of a solution of DIC (0.63 g, 4.99 mmol) in 1,2-dichloropropane (5 ml). The mixture was shaken at room temperature for 15 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) and a solution of 1-methyl-4-methylaminopiperidine (0.10 g, 0.78 mmol) in 1,2-dichloropropane (10 ml). The resulting mixture was shaken at room temperature for 21 hours and then at 60° C. for one hour, filtered, and the polymer was carefully washed with DCM and methanol. The combined filtrates were concentrated to yield the crude product, which was purified by column chromatography (silicagel, gradient elution with DCM/methanol). The amine was mixed with ethanol and 1 molar aqueous hydrochloric acid, concentrated, and the residual hydrochloride was recrystallized from acetone. 120 mg (42%) of the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767695B2
Source datasetuspto-grants-2010_08
ORD IDord-52d7dd6105434f9b870516259c65cab8
Source noteuspto-grants-2010_08