참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethylaluminum chloride | HCID 7277 | — |
| 반응물 | 2,6-Lutidine | HCID 7937 | — |
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | Quinoxaline-6-carbonyl chloride | HCID 2776328 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(6-Methylpyridin-2-yl)-1-(quinoxalin-6-yl)ethanone | HCID 22394529 | 60.8% |
반응 단계
A stirred solution of 2,6-lutidine (1.4 g, 13 mmole) in dry THF (100 ml) at −60° C. under Ar was treated dropwise with a solution of BuLi in hexane (2.5 M, 5.2 ml, 13 mmole). After 30 mins a solution of Et2AlCl in hexane (14 ml, 14 mmole) was added dropwise and the solution warmed to 20° C. After a further 30 mins the solution was cooled to −50° C. and transferred via canula to a stirred solution of quinoxaline-6-carbonyl chloride (2.0 g, 10.3 mmole) in THF (100 ml) at −60° C. Stirring was continued for 20 min and the solution quenched with sat. aq. NH4Cl solution and warmed to 20° C. The mixture was filtered through Kieselguhr and the filtrate worked up as normal (EtOAc, water, Na2SO4). Filtration through silica eluting with EtOAc gave the product as a yellow solid (1.65 g, 51%). m/z [ESMS]: 264 [M+H]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06906089B2 |
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| 출처 데이터셋 | uspto-grants-2005_06 |
|---|
| ORD ID | ord-0e47f117d90f470e9175b38f4ebf4cb3 |
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| 출처 메모 | uspto-grants-2005_06 |
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