참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | Ammonium dithiocarbamate | HCID 11083854 | — |
| 반응물 | Ethylbromopyruvate | HCID 21948992 | — |
| 생성물 | HCID 178470113 | HCID 178470113 | — |
반응 단계
Ethylbromopyruvate (7.1 mL, 56.8 mmol) was added to a slurry of ammonium dithiocarbamate (6.25 g, 56.8 mmol) in EtOH (35 mL). The solution was stirred at rt 18 h, then heated at 70°-80° C. for 2 h. The solution was cooled to 10° C. and water (70 mL) was added. The resulting precipitate was recrystallized from EtOH to give 0.7 g of 4-carboethoxy-2-mercapto thiazole. NCS (0.42 g, 3.17 mmol) was added to a solution of 4-carboethoxy-2-mercapto thiazole (0.15 g, 0.79 mmol) in CH2Cl2 (3.2 mL) and the solution layered with water (1.6 mL) and stirred for 2 h. The layers were separated and the water layer extracted with CH2Cl2. The combined extracts were concentrated and the residue dissolved in acetone (1 mL) and NH4OH (1.6 mL) added. After 5 min the acetone was removed in vacuo and the residue taken up in water and extracted with EtOAc (6×5 mL). The combined extracts were dried (MgSO4), filtered, concentrated and purified by chromatography using 35% EtOAc/hexane to give 0.1 g (54%) 4-carboethoxy-2-thiazole sulfonamide as a pale yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05519040 |
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| 출처 데이터셋 | uspto-grants-1996_05 |
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| ORD ID | ord-10a9172f6ff54bdc9813b75d7be8129e |
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| 출처 메모 | uspto-grants-1996_05 |
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