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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045361Generated: October 25, 2026

Acetic Acid → HCID 44124557, compound

https://huagongshe.com/reaction/1045361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-Hydroxy-4-(6-methoxypyridin-3-YL)cyclohexanoneHCID 52987995—
ReactantHCID 59569566HCID 59569566—
Solvent1,1-DichloroethaneHCID 6365—
SolventEthyl AcetateHCID 8857—
ProductHCID 44124557HCID 44124557—

Reaction Steps

The title compound was prepared according to general procedures described in Scheme 2: A mixture of 4-hydroxy-4-(6-methoxypyridin-3-yl)cyclohexanone (71 mg, 0.32 mmol), (3-(methoxymethyl)pyrrolidin-3-yl)(3-(trifluoromethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)methanone VIc (100 mg, 0.29 mmol) and acetic acid (20 μL, 0.34 mmol) in dichloroethane (3 mL) was stirred at room temperature for 0.5 h. Sodium triacetoxyborohydride (123 mg, 0.576 mmol) was added and the reaction mixture was stirred for 2 h at room temperature. After concentration of solvent under reduced pressure, the resulting residue was dissolved in ethyl acetate, then washed with NaHCO3, water and brine. The organic extract was dried, filtered and concentrated. The crude product was obtained as a mixture of isomers which were further separated by reverse phase preparative HPLC to yield isomer A (eluted at 10.092 min) and isomer B (eluted at 11.269 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569282B2
Source datasetuspto-grants-2013_10
ORD IDord-6ed87c0d32184f9894cffe87565e1073
Source noteuspto-grants-2013_10