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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829712Generated: November 4, 2026

Hydrochloric Acid → HCID 22054643, compound

https://huagongshe.com/reaction/1829712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFelbinacHCID 3332—
Reactant2-NitrophenolHCID 6947—
ReactantDiisopropylcarbodiimideHCID 12734—
Reactant4-(1-Pyrrolidinyl)piperidineHCID 78703—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
Solvent1,2-DichloropropaneHCID 6564—
ProductHCID 22054643HCID 2205464329%

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 4-(1-pyrrolidinyl)piperidine (0.123 g, 0.80 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 mixed with ethanol and 1 molar aqueous hydrochloric acid, concentrated, and the residual hydrochloride was recrystallized from ethanol. 90 mg (29%) of the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064135B2
Source datasetuspto-grants-2006_06
ORD IDord-b088907e24a64a038b49f39512bc6ea8
Source noteuspto-grants-2006_06