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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275422생성일: 2026년 10월 27일

Acetonitrile → (3S-trans)-[2-[(6-Cyano-3,4-dihydro-3-hydroxy-2,2-dimethyl-2H-pyran-4yl)amino]phenyl]carbamic acid, ethyl ester

https://huagongshe.com/reaction/275422

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Magnesium perchlorateHCID 24840—
반응물(1aS,7bS)-2,2-Dimethyl-1a,7b-dihydro-2H-oxireno[2,3-c]chromene-6-carbonitrileHCID 9837089—
반응물2-[(Ethoxycarbonyl)amino]anilineHCID 12215006—
용매Ethyl AcetateHCID 8857—
생성물(3S-trans)-[2-[(6-Cyano-3,4-dihydro-3-hydroxy-2,2-dimethyl-2H-pyran-4yl)amino]phenyl]carbamic acid, ethyl esterHCID 6784519092.8%

반응 단계

The reaction mixture containing (1aS-cis)-1a,7b-dihydro-2,2-dimethyl-2H-oxireno-[c][1]benzopyran-6-carbonitrile, from example 2, part A (1.0 g, 5.0 mmol), 2-[(ethoxycarbonyl)amino]aniline, compound of example 1, part B (900 mg, 5.0 mmol) and magnesium perchlorate (1.12 g, 5.0 mmol) in acetonitrile (5.0 mL) was stirred under argon at room temperature for 48 hours. The reaction mixture was diluted with ethyl acetate and washed with water, saturated sodium bicarbonate solution and brine. After drying over anhydrous magnesium sulfate, the solvent was evaporated to give a colorless foam which was purified by flash chromatography (25% ethyl acetate in hexanes) to yield the title product as an amorphous solid (1.76 g, 92.8%) (shrinks at 84° C.). [a]D =+21° (c=1.1%, MeOH). Microanalysis calculated for C21H23N3O4 : C,66.13; H, 6.08; N,11.02. Found: C, 66.11 ; H, 6.15; N, 10.78.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05393771
출처 데이터셋uspto-grants-1995_02
ORD IDord-57fd679929ab417a953abb3ddfc20d6a
출처 메모uspto-grants-1995_02