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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1864591생성일: 2026년 10월 23일

Boron tribromide → [2-(4-acetamidophenylsulfanyl)-7-hydroxy-quinazolin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine

https://huagongshe.com/ko/reaction/1864591

반응식

참여 물질

역할이름HCID투입량
반응물Boron tribromideHCID 25134—
반응물HCID 178418798HCID 178418798—
용매DichloromethaneHCID 6344—
용매1,1-DichloroethaneHCID 6365—
생성물[2-(4-acetamidophenylsulfanyl)-7-hydroxy-quinazolin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amineHCID 178418855—

반응 조건

온도80 °C

반응 단계

A solution of [2-(4-acetamidophenylsulfanyl)-7-methoxy-quinazolin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine (23 mg, 5.54.10−5 mol) in dichloroethane (3 mL) is treated with 1M BBr3 in dichloromethane (222 μL, 2.21.10−4 mol). The mixture of heated at 80° C. for 4 hours before 1M BBr3 in DCM (222 μL, 2.21.10−4 mol) is added. The reaction mixture is heated at 80° C. for a further 3 hours. The solvent is evaporated and methanol is added to the residue to quench residual BBr3. The solvent is evaporated in vacuo and this operation repeated 3 times. 1M HCl (2 mL) is added to the solid residue and the suspension stirred at room temperature for 15 hours. The solid is collected by filtration and suspended in a mixture water/EtOH (3/1, 8 mL). The mixture is neutralized with NaHCO3 and stirred for 2 hours at room temperature. The solid is then collected by filtration, rinsed with water and diethyl ether to give the desired [2-(4-acetamidophenylsulfanyl)-7-hydroxy-quinazolin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07625913B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-ff62038026b646ffa39b093dabe7f7d2
출처 메모uspto-grants-2009_12