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HRID 1486241Erstellt: 26. Oktober 2026

Triphenylphosphine → Ethyl 2,5-dimethyl-7-[(2,3,6-trifluorobenzyl)oxy]pyrazolo[1,5-a]pyridine-3-carboxylate

https://huagongshe.com/reaction/1486241

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Edukt2,3,6-Trifluorobenzyl alcoholHCID 145500—
EduktDiisopropyl azodicarboxylateHCID 5363146—
EduktHCID 178469270HCID 178469270—
LösungsmittelTetrahydrofuranHCID 8028—
Lösungsmitteltert-Butyl methyl etherHCID 15413—
ProduktEthyl 2,5-dimethyl-7-[(2,3,6-trifluorobenzyl)oxy]pyrazolo[1,5-a]pyridine-3-carboxylateHCID 11785976360,4%

Reaktionsschritte

1.2 g (5.25 mmol) of ethyl 7-hydroxy-2,5-dimethylpyrazolo[1,5-a]pyridine-3-carboxylate from Example 8A were dissolved in 48 ml of THF. 1.7 g (10.50 mmol) of 2,3,6-trifluorobenzyl alcohol and 2.9 g (11.03 mmol) of triphenylphosphine were added. Subsequently, 2.2 ml (11.03 mmol) of diisopropyl (E)-diazene-1,2-dicarboxylate were added to the solution, which was stirred at RT for 1 h. 120 ml of tert-butyl methyl ether were added, then the mixture was stirred briefly, and the solids formed were filtered off and dried under high vacuum. 1.2 g of the target compound were obtained (62% of theory).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09422285B2
Quelldatensatzuspto-grants-2016_08
ORD IDord-46521d68c9e846b49e694be7013db26e
Quellennotizuspto-grants-2016_08