Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7392생성일: 2026년 10월 24일
Sodium Iodide → 1-(cyclopropylmethyl)-3-(beta-D-glucopyranosyloxy)-5-methyl-4-[(4methylthiophenyl)methyl]-1H-pyrazole
https://huagongshe.com/ko/reaction/7392
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | Bromomethylcyclopropane | HCID 81503 | — |
| 반응물 | 3-(beta-D-glucopyranosyloxy)-5-methyl-4-[(4-methylthiophenyl)methyl]-1H-pyrazole | HCID 9952610 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-(cyclopropylmethyl)-3-(beta-D-glucopyranosyloxy)-5-methyl-4-[(4methylthiophenyl)methyl]-1H-pyrazole | HCID 23545514 | — |
반응 단계
To a solution of 3-(β-D-glucopyranosyloxy)-5-methyl-4-[(4-methylthiophenyl)methyl]-1H-pyrazole (0.081 g) in N,N-dimethylformamide (1 mL) were added cesium carbonate (0.40 g), bromomethylcyclopropane (0.099 mL) and a catalytic amount of sodium iodide, and the mixture was stirred at room temperature for 7 days. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: dichloromethane/methanol=10/1-8/1) to give 1-(cyclopropylmethyl)-3-(β-D-glucopyranosyloxy)-5-methyl-4-[(4methylthiophenyl)methyl]-1H-pyrazole (0.041 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07087579B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-18c5dd7d2c2244d79595acf160ae3565 |
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| 출처 메모 | uspto-grants-2006_08 |
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