참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 반응물 | 5-Bromo-3-(2-triethylsilylethynyl)pyrazin-2-amine | HCID 86675702 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 생성물 | 2-bromo-5H-pyrrolo[2,3-b]pyrazine | HCID 25067308 | 70.3% |
반응 단계
Potassium tert-butoxide (6.612 g, 58.92 mmol) was suspended/dissolved in dry N-methylpyrrolidinone (15 mL) and stirred at 80° C. while a solution of 5-bromo-3-(2-triethylsilylethynyl)pyrazin-2-amine (9.1992 g, 29.46 mmol) in dry N-methylpyrrolidinone (50 mL) was added slowly drop wise over 10 minutes. The dropping funnel was washed out with a further aliquot of dry N-methylpyrrolidinone (10 mL). The resultant was stirred at 80° C. for 1.5 hours. Reaction mixture cooled to ambient then diluted with EtOAc and water and EtOAc layer washed with small portions of water (×6). Organic layer dried (MgSO4), filtered and concentrated in vacuo to give a dark brown solid (4.1 g, 70.3%). 1H NMR (400.0 MHz, DMSO) δ 12.50 (s, 1H), 8.37 (s, 1H), 8.01 (s, 1H) and 6.64 (q, J=1.7 Hz, 1H) ppm; MS (ES+) 198.10.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08822469B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-0ff2bc3b68aa4673910b8a5cd4c05079 |
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| 출처 메모 | uspto-grants-2014_09 |
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