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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2048544생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2048544

반응식

참여 물질

역할이름HCID투입량
반응물AmitroleHCID 1639—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물cis-2,6-dimethyloxan-4-oneHCID 10441716—
용매Acetic AcidHCID 176—
생성물N-[(2R,6S)-2,6-dimethyltetrahydro-2H-pyran-4-yl]-1H-1,2,4-triazol-5-amineHCID 6700874049%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08592431B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-cf54a492207746d28cc5958667bcf864
출처 메모uspto-grants-2013_11