참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | Imidazo[1,2-a]pyridine,5-[(4-chlorobutyl)thio]- | HCID 18936641 | — |
| 반응물 | Oxazolidine-2,4-dione potassium salt | HCID 70204806 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-[4-(Imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dione | HCID 18936736 | — |
반응 단계
To a solution of 6.30 g (26.2 mmol) of 5-(4-chlorobutylthio)imidazo[1,2-a]pyridine and 3.64 g (26.2 mmol) of oxazolidine-2,4-dione potassium salt in 100 ml of N,N-dimethylformamide, 3.92 g (26.2 mmol) of sodium iodide was added, followed by stirring at 80° C. for 16 hours. After cooling, the reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with water and dried, after which the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to yield 5.70 g (71.4%, light orange crystal) of the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05840732 |
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| 출처 데이터셋 | uspto-grants-1998_11 |
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| ORD ID | ord-27485b8152fb4f81a5a886d5a64aeede |
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| 출처 메모 | uspto-grants-1998_11 |
|---|