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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594901Generated: October 30, 2026

18-Crown-6 → HCID 178435251, compound

https://huagongshe.com/reaction/1594901

Reaction equation

Participants

RoleNameHCIDCharge
Reactant18-Crown-6HCID 28557—
ReactantPotassium FluorideHCID 522689—
Reactant3-Ethylhexahydro-3-(3-hydroxyphenyl)-1-methyl-2H-azepin-2-oneHCID 2794573—
Reactant4-(4-Cyano-3-fluoro-phenyl)-6,7-dihydro-4h-imidazo [4,5-c]pyridine-3,5-dicarboxylic acid di-tert-butyl esterHCID 54044207—
SolventAcetonitrileHCID 6342—
ProductHCID 178435251HCID 178435251—

Reaction Steps

4-(4-Cyano-3-fluoro-phenyl)-6,7-dihydro-4H-imidazo[4,5-c]pyridine-3,5-dicarboxylic acid di-tert-butyl ester (as described above in Step B) (0.120 g, 0.270 mmol), 3-ethyl-3-(3-hydroxy-phenyl)-1-methyl-azepan-2-one (0.067 g, 0.270 mmol), KF.Al2O3 (0.080 g) and 18-Crown-6 (0.007 g) were refluxed in CH3CN (5 mL) under Ar for 24 h. The solution was filtered and concentrated in vacuo. The residue was dissolved in CH2Cl2 (10 mL) and TFA (5 mL) and stirred at RT for ½ h. The solution was concentrated in vacuo, purified using reverse phase chromatography (95/5 to 5/95 H2O/CH3CN w/0.1% TFA, flow=65 mL/min), lyophilized, and then further separated into two diastereomers using a Chiralpak AS column.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06284755B1
Source datasetuspto-grants-2001_09
ORD IDord-64933a4464a84314a4561094285028fd
Source noteuspto-grants-2001_09