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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408125Generated: November 2, 2026

Isobutylene → HCID 70496562, compound

https://huagongshe.com/reaction/2408125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyleneHCID 8255—
Reactant3-Chloro-4-fluorobenzaldehydeHCID 593866—
ReactantYtterbium triflateHCID 2733225—
Reactant5-Aminopyridine-2-carbonitrileHCID 3871395—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 70496562HCID 704965625%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred solution of 5-amino-pyridine-2-carbonitrile (9.3 g, 78.4 mmol) and 3-chloro-4-fluoro-benzaldehyde (12.3 g, 78.4 mmol) in acetonitrile (150 mL) were added isobutene (21.0 mL, 313.5 mmol) and ytterbium(III) trifluoromethanesulfonate (Yb(OTf)3) (5.8 g, 9.5 mmol). The resulting mixture was stirred at 85° C. for 18 h in sealed tube. The mixture was diluted with ethyl acetate (300 mL) and washed with water (100 mL×2) and brine (100 mL×2) and then dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by ISCO combi-flash chromatography (gradient elution, 10-50% ethyl acetate in petroleum ether) to afford 2-(3-chloro-4-fluoro-phenyl)-4,4-dimethyl-1,2,3,4-tetrahydro-[1,7]naphthyridine-6-carbonitrile (1.2 g, 5.0%) as a light yellow solid: MS (ESI) M+1=316.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809369B2
Source datasetuspto-grants-2014_08
ORD IDord-1793daeb0daa4dda90010066064ff173
Source noteuspto-grants-2014_08