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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

반응식

참여 물질

역할이름HCID투입량
반응물MagnesiumHCID 5462224—
반응물(3-Bromophenethoxy)(tert-butyl)dimethylsilaneHCID 11515183—
반응물5-Amino-1-(4-fluorophenyl)4-(2-pyridylthiocarboxy)pyrazoleHCID 53787978—
용매TetrahydrofuranHCID 8028—
생성물5-Amino-1-(4-fluorophenyl)-4-[3-(2-tert-butyldimethylsiloxyethyl)benzoyl]pyrazoleHCID 1160458435.9%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06376527B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-5a505cf3240a4d159af2e7c71b6bba65
출처 메모uspto-grants-2002_04