참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Aminopyrimidine | HCID 7978 | — |
| 반응물 | 2-Bromo-1-(4-hydroxy-3-methoxyphenyl)ethan-1-one | HCID 13542258 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 2-(4-Hydroxy-3-methoxyphenyl)imidazo[1,2-a]pyrimidine | HCID 69810456 | 62.2% |
반응 단계
To 30 ml of an acetonitrile solution of 3.9 g (16 mmol) of 4′-hydroxy-3′-methoxy-2-bromoacetophenone was added 3.2 g (34 mmol) of 2-aminopyrimidine, and the mixture was stirred at 65° C. for 2 hours. The precipitated crystals were suction filtered and dissolved in 100 ml of 50% methanol. This solution was mixed with 1.3 g of sodium hydrogencarbonate and stirred at room temperature for 10 minutes. The precipitated crystals were suction filtered, and recrystallized from 50 ml of 50% methanol, thereby giving 2.4 g of 2-(4-hydroxy-3-methoxyphenyl)imidazo[1,2-a]pyrimidine in an yield of 62%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08895599B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-59315116c28b4b959b943af348105111 |
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| 출처 메모 | uspto-grants-2014_11 |
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