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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Trimethylsilyl cyanide | HCID 82115 | — |
| 반응물 | 3-Oxetanone | HCID 15024254 | — |
| 반응물 | N-((7-amino-8-benzyl-5,6,7,8-tetrahydronaphthalen-2-yl)methyl)ethanesulfonamide | HCID 86685687 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | N-((8-Benzyl-7-(3-cyanooxetan-3-ylamino)-5,6,7,8-tetrahydronaphthalen-2-yl)methyl)ethanesulfonamide | HCID 71572158 | 2.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08846741B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-72761eb1556941b5aaf627974e53d02c |
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| 출처 메모 | uspto-grants-2014_09 |
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