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HRID 1412515作成日:2026年10月26日

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

https://huagongshe.com/reaction/1412515

反応式

関与物質

役割名称HCID仕込み量
反応物AmitroleHCID 1639—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物cis-2,6-dimethyloxan-4-oneHCID 10441716—
溶媒Acetic AcidHCID 176—
生成物N-[(2R,6S)-2,6-dimethyltetrahydro-2H-pyran-4-yl]-1H-1,2,4-triazol-5-amineHCID 6700874049%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08921379B2
出典データセットuspto-grants-2014_12
ORD IDord-feac67a911d3488099fb98ed3db8c4ca
出典メモuspto-grants-2014_12