Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 843067생성일: 2026년 10월 26일
Magnesium → 5-Amino-1-(4-fluorophenyl)-4-[3-(2-tert-butyldimethylsiloxyethyl)benzoyl]pyrazole
https://huagongshe.com/reaction/843067
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Magnesium | HCID 5462224 | — |
| 반응물 | (3-Bromophenethoxy)(tert-butyl)dimethylsilane | HCID 11515183 | — |
| 반응물 | 5-Amino-1-(4-fluorophenyl)4-(2-pyridylthiocarboxy)pyrazole | HCID 53787978 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-Amino-1-(4-fluorophenyl)-4-[3-(2-tert-butyldimethylsiloxyethyl)benzoyl]pyrazole | HCID 11604584 | 35.9% |
반응 단계
Into an oven dried flask containing magnesium turnings (0.386 g, 15.9 mmol) and tetrahydrofuran (10 ml) was added 3-(2-tert-butyldimethylsiloxyethyl)bromobenzene (5.0 g, 15.9 mmol) and the reaction mixture was heated at reflux. After 3 h, the reaction mixture was cooled to room temperature and 5-amino-1-(4-fluorophenyl)-4-(2-pyridylthiocarboxy)pyrazole (2.37 g, 7.6 mmol) was added and the stirring was continued for 16 h. The reaction mixture was concentrated in vacuo. The residue was dissolved in ethyl acetate and washed with aqueous ammonium chloride and brine and dried over sodium sulfate. The organics were removed in vacuo and the residue was purified by flash chromatography (elution gradient: 10-30% ethyl acetate/hexane) to give 5-amino-1-(4-fluorophenyl)-4-[3-(2-tert-butyldimethylsiloxyethyl)benzoyl]pyrazole (1.20 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06376527B1 |
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| 출처 데이터셋 | uspto-grants-2002_04 |
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| ORD ID | ord-5a505cf3240a4d159af2e7c71b6bba65 |
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| 출처 메모 | uspto-grants-2002_04 |
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