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HRID 1497747Erstellt: 25. Oktober 2026

Diisopropylethylamine → 6-Bromo-7-methyl-8-(3-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine

https://huagongshe.com/reaction/1497747

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktEthyl isothiocyanatoformateHCID 85320—
EduktHydroxyamine hydrochlorideHCID 443297—
Edukt5-Bromo-4-methyl-3-(3-trifluoromethyl-phenyl)-pyridin-2-ylamineHCID 86708086—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt6-Bromo-7-methyl-8-(3-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamineHCID 8670808785,4%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

5-Bromo-4-methyl-3-(3-trifluoromethyl-phenyl)-pyridin-2-ylamine (Int. 1, 12.0 g, 36.25 mmol) was stirred in dioxane (250 mL) at RT and ethoxycarbonyl isothiocyanate (4.27 mL, 36.25 mmol) was added dropwise. The reaction mixture was stirred for 18 hrs, then the solvent was evaporated in vacuo. The resultant residue was dissolved in MeOH/IMS (1:1, 460 mL) and hydroxylamine hydrochloride (12.58 g, 181 mmol) was added and the reaction mixture was heated to 60° C. DIPEA (18.6 mL, 109 mmol) was added, and the reaction mixture was heated for a further 4.5 rs before allowing to cool. The resultant precipitate was collected by filtration, washed with MeOH and dried to afford the title compound as a white solid (11.49 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09199984B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-5b2d169b69bb49e0a314189f2b5f052d
Quellennotizuspto-grants-2015_12