Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324415생성일: 2026년 10월 26일
Boron trifluoride etherate → (+/-)-5-(7-Ethyl-9,10-dihydro-2-methyl-4H-benzo[5,6]cyclohepta[1,2-d]oxazol-4-yl)-2,4(1H,3H)-pyrimidinedione
https://huagongshe.com/reaction/324415
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Boron trifluoride etherate | HCID 8000 | — |
| 반응물 | Triethylsilane | HCID 12052 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | (+/-)-4-(2,4-Bis(1,1-dimethylethoxy)pyrimidin-5-yl)-7-ethyl-2-methyl-9,10-dihydro-4H-benzo[5,6]cyclohepta[1,2-d]oxazol-4-ol | HCID 70113732 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (+/-)-5-(7-Ethyl-9,10-dihydro-2-methyl-4H-benzo[5,6]cyclohepta[1,2-d]oxazol-4-yl)-2,4(1H,3H)-pyrimidinedione | HCID 70114236 | — |
반응 단계
A stirred solution of the product from step (i) (0.60 g) in dichloromethane (15 ml) was treated with triethylsilane (0.225 ml) and cooled to 0° C. Boron trifluoride etherate (0.65 ml) was added in four equal portions at 5 minute intervals and the reaction stirred at room temperature for 16 hours. The reaction was poured into saturated sodium bicarbonate solution (200 ml) and extracted with ethyl acetate. The extracts were dried (MgSO4) and evaporated to give a yellow solid which was purified by reverse phase chromatography eluting with 50% to 80% methanol in 0.1% aqueous ammonium acetate.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06218376B1 |
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| 출처 데이터셋 | uspto-grants-2001_04 |
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| ORD ID | ord-81e57e3676454468b17fdd38b48e4ab2 |
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| 출처 메모 | uspto-grants-2001_04 |
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