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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246887Generated: October 30, 2026

Trifluoroacetic acid → HCID 12108348, compound

https://huagongshe.com/reaction/1246887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3-PyridinecarboxaldehydeHCID 10371—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-(1-Boc-piperidin-3-ylmethyl)-N-phenyl-propionamideHCID 12991578—
SolventDichloromethaneHCID 6344—
ProductHCID 12108348HCID 1210834876%

Reaction Steps

Trifluoroacetic acid (0.5 mL) was added dropwise to a solution of N-(1-Boc-piperidin-3-ylmethyl)-N-phenyl-propionamide 5 (21 mg, 0.061 mmol) in 0.5 mL of dry CH2Cl2 at 0° C. (ice-water). The reaction mixture was stirred at room temperature for 30 minutes. TLC showed the reaction was complete. After removal of the solvents, the residue was dried under vacuum for 3 hrs. The crude compound was dissolved in DMF (0.5 mL) and 3-pyridine carboxaldehyde (8.6 μL, 1.5 eq.) was added. The mixture was stirred at room temperature for 30 min. NaB(OAc)3H (95%, 20.3 mg, 1.5 eq.) was introduced in one portion, and the mixture was shaken at room temperature overnight. The mixture was quenched with 5 mL of aqueous potassium carbonate (sat.), then extracted with ethyl acetate (3×10 mL). The extracts were combined and washed with aqueous NaHCO3 (sat., 2×5 μL), brine (10 mL), and dried over anhydrous sodium sulfate. After the solvent was removed, the remaining oily residue was purified by preparative thin layer chromatography (EtOAc/MeOH, 9:1) to afford N-[1-(Pyridin-3-ylmethyl)-piperidin-3-ylmethyl]-N-phenyl-propionamide 12 as a colorless oil (15.6 mg, 76%). LRMS 338.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129228B2
Source datasetuspto-grants-2006_10
ORD IDord-64b605ffcf004539a74279fd7c0cec06
Source noteuspto-grants-2006_10