참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Thiobenzamide | HCID 683563 | — |
| 반응물 | 2-Bromo-1-(2-phenylpyrimidin-5-yl)ethanone | HCID 59252454 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 2-Phenyl-4-(2-phenylpyrimidin-5-yl)thiazole | HCID 59252447 | 46% |
반응 단계
A mixture consisting of 2-bromo-1-(2-phenylpyrimidin-5-yl)ethanone (Example 14, Step B, 50 mg, 0.18 mmol), thiobenzamide (TCl America, 25 mg, 0.18 mmol) and absolute ethanol (4 mL) in a capped scintillation vial was heated to near boiling for several minutes and was subsequently allowed to cool to room temperature. A white solid precipitated within minutes. The precipitate was collected by vacuum filtration. Light ethanol rinse, suction, and drying under high vacuum at room temperature afforded the title compound (26 mg, 46% yield) as an off-white solid; melting point 214.4-216.1° C.; 1H-NMR (400 MHz; DMSO-d6) δ 9.54 (s, 2H), 8.54 (s, 1H), 8.47 (m, 2H), 8.08 (m, 2H), 7.62-7.54 (m, 6H); LC/MS (ESI+) m/z 316.1, (ESI−) m/z 337.2 (M−1+Na+); H-PGDS FPBA IC50: >20 μM.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08536185B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-59b63460ac33409aa614d4fadb29ae68 |
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| 출처 메모 | uspto-grants-2013_09 |
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