참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl bromopyruvate | HCID 66144 | — |
| 반응물 | Pyridine-2-carbothioamide | HCID 1549499 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | Ethyl 2-pyridin-2-yl-1,3-thiazole-4-carboxylate | HCID 10082761 | 35.4% |
반응 단계
A solution of the product of Example 3H (25.4 mmol) in ethanol (50 mL) was treated with ethyl bromopyruvate (3 mL, 23.9 mmol) and molecular sieves (10 g, 3 Å), heated at reflux for 16 hours, cooled to 25° C., filtered and concentrated. The concentrate was partitioned between ethyl acetate and saturated NaHCO3, and the organic phase was washed with brine, dried over MgSO4, filtered and concentrated. The residue was chromatographed on silica gel eluting with 0-25% ethyl acetate in dichloromethane to give the title compound (1.98 g, 33% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07834043B2 |
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| 출처 데이터셋 | uspto-grants-2010_11 |
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| ORD ID | ord-7a125277526f45339d6f7ae805fcaa7b |
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| 출처 메모 | uspto-grants-2010_11 |
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