참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Trimethylsilyl cyanide | HCID 82115 | — |
| 반응물 | 3-(benzyloxy)-5-bromopyridine N-oxide | HCID 58213489 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 5-(Benzyloxy)-3-bromopicolinonitrile | HCID 67117707 | — |
반응 단계
To a solution of 53-(benzyloxy)-5-bromopyridine 1-oxide (from step 2) (1.0 eq.) in acetonitrile (0.2 M) was added trimethylsilyl cyanide (TMSCN) (4.0 eq.) and triethylamine (3.0 eq.). The reaction was heated at 100° C. overnight. After cooling to room temperature, the solvent was concentrated en vacuo, and the residue was purified by a COMBIFLASH® system (ISCO) using 0-40% ethyl acetate in hexane to give a mixture of two benzoxy regioisomers, one of which was the desired product. The mixture was carried onto the next step without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08895577B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-79c3e6c71bb74976b38875d78721c99b |
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| 출처 메모 | uspto-grants-2014_11 |
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