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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 82872생성일: 2026년 10월 23일

Trimethylsilyl cyanide → N-((8-Benzyl-7-(3-cyanooxetan-3-ylamino)-5,6,7,8-tetrahydronaphthalen-2-yl)methyl)ethanesulfonamide

https://huagongshe.com/ko/reaction/82872

반응식

참여 물질

역할이름HCID투입량
반응물Trimethylsilyl cyanideHCID 82115—
반응물3-OxetanoneHCID 15024254—
반응물N-((7-amino-8-benzyl-5,6,7,8-tetrahydronaphthalen-2-yl)methyl)ethanesulfonamideHCID 86685687—
용매Ethyl AcetateHCID 8857—
생성물N-((8-Benzyl-7-(3-cyanooxetan-3-ylamino)-5,6,7,8-tetrahydronaphthalen-2-yl)methyl)ethanesulfonamideHCID 715721582.4%

반응 조건

온도210 °C

반응 단계

N-((7-Amino-8-benzyl-5,6,7,8-tetrahydronaphthalen-2-yl)methyl)ethanesulfonamide (0.243 g, 0.678 mmol) and 3-oxetanone (0.098 g, 1.356 mmol) were sealed in a vial and heated at 210° C. for 2 minutes. Trimethylsilyl cyanide (0.181 mL, 1.356 mmol) was added, the vial was resealed and the mixture was heated again at 210° C. for 2 minutes. The mixture was diluted with ethyl acetate (40 mL) and washed with 1 N NaOH (1×20 mL) and brine (1×20 mL). The organic extract was collected, dried on MgSO4 and evaporated under reduced pressure to give a brown oil. The residue was purified by preparative HPLC. Product was obtained as a colourless oil (7.2 mg, 0.016 mmol, 2.4%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846741B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-72761eb1556941b5aaf627974e53d02c
출처 메모uspto-grants-2014_09