戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 519804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/519804

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US09115136B2
出典データセットuspto-grants-2015_08
ORD IDord-597caf5348ae442e8ad6c22644bf03d0
出典メモuspto-grants-2015_08