참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dichloromethane methanol | HCID 21226129 | — |
| 반응물 | 2,4-Dichloro-5-methoxy-6-vinylpyrimidine | HCID 86689326 | — |
| 생성물 | 2,6-Dichloro-5-methoxypyrimidine-4-carbaldehyde | HCID 86689330 | 100% |
반응 단계
The solution of 2,6-dichloro-5-methoxy-4-vinyl pyrimidine (50 g, 0.24 mol) in dichloromethane:methanol (4:1, 2 L), prepared by Example 1, was cooled to −78° C. Ozone gas was bubbled through for 5 h. The reaction was quenched with dimethyl sulfide (50 mL). The mixture was slowly warmed to room temperature and concentrated under reduced pressure at 40° C. to provide a crude material comprising the title compound (50.5 g, 100% yield); HPLC (85% acetonitrile buffered with 0.1% v/v acetic acid. The title compound was not isolated from the crude material.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08877925B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-012f2a2c013c4e5a8396870fe1076f20 |
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| 출처 메모 | uspto-grants-2014_11 |
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