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HRID 1688770Erstellt: 26. Oktober 2026

Amitrole → N-[(2R,6S)-2,6-dimethyltetrahydro-2H-pyran-4-yl]-1H-1,2,4-triazol-5-amine

https://huagongshe.com/reaction/1688770

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmitroleHCID 1639—
EduktSodium triacetoxyborohydrideHCID 5049666—
Eduktcis-2,6-dimethyloxan-4-oneHCID 10441716—
LösungsmittelAcetic AcidHCID 176—
ProduktN-[(2R,6S)-2,6-dimethyltetrahydro-2H-pyran-4-yl]-1H-1,2,4-triazol-5-amineHCID 6700874049%

Reaktionsschritte

To a solution of 1H-1,2,4-triazol-5-amine (1.6 g) in acetic acid (30 mL) was added (2R,6S)-2,6-dimethyltetrahydro-4H-pyran-4-one (2.5 g) at room temperature, and the mixture was stirred for 30 min. After stirring, sodium triacetoxyborohydride (5.2 g) was added, and the mixture was stirred at room temperature for 20 hr. Acetic acid was evaporated and ethyl acetate and water were added to the residue. The mixture was neutralized with sodium hydrogen carbonate, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated. The residue was dissolved in a small amount of ethyl acetate, and the mixture was crystallized from diisopropyl ether. The resulting solid was collected by filtration, washed with diisopropyl ether, and dried by heating under reduced pressure to give the title compound as a pale-yellow solid (1.6 g, 49%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08148383B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-c605c14f304943a89e1d4d3365adcadf
Quellennotizuspto-grants-2012_04