Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | HCID 11344780 | HCID 11344780 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22667816 | HCID 22667816 | — |
Reaction Steps
400 mg of 2-chloro-4,5-dihydro-6H-imidazo[4,5,1-ij]quinolin-6-one in 5 mL of dimethylformamide, 70 mg of potassium fluoride, 0.2 mL of 2,6-lutidine and 1.6 g of 4-(N-methylpiperidinium)piperidine chloride are added to a three-necked flask under argon and left stirring for 5 hours at 140° C. The mixture is evaporated on a vacuum pump and the residue obtained is chromatographed with 70 g of Silica H (Merck) (eluent: dichloromethane with 10% methanol and 0.5% triethylamine). 50 mg of pure product are obtained, the NMR spectrum of which corresponds to the desired structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06794382B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-d6feb179a2044811962e674c903d67b0 |
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| Source note | uspto-grants-2004_09 |
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