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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7615생성일: 2026년 10월 23일

Boron tribromide → [2-(4-acetamido-phenyl-sulfanyl)-6-(4-hydroxyphenyl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine

https://huagongshe.com/ko/reaction/7615

반응식

참여 물질

역할이름HCID투입량
반응물Boron tribromideHCID 25134—
반응물HCID 178418826HCID 178418826—
용매DichloromethaneHCID 6344—
용매1,1-DichloroethaneHCID 6365—
생성물[2-(4-acetamido-phenyl-sulfanyl)-6-(4-hydroxyphenyl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amineHCID 178418864—

반응 조건

온도80 °C

반응 단계

A solution of [2-(4-acetamido-phenyl-sulfanyl)-6-(4-methoxyphenyl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine (100 mg, 2.24.10−4 mol) in dichloroethane (5 mL) is treated with 1M BBr3 in DCM (896 μL, 8.96.10−4 mol). The mixture is then heated at 80° C. for 4 hours before 1M BBr3 in DCM (896 μL, 8.96.10−4 mol) is added. The reaction mixture is then heated at 80° C. for a further 3 hours. The solvent is evaporated and methanol is added to the residue to quench any residual BBr3. The solvent is evaporated in vacuo and this evaporation step is repeated 3 times. 1M HCl(8 mL) is added to the solid residue and the suspension is stirred at room temperature for 15 hours. The solid is collected by filtration and suspended in a mixture of water/EtOH (3/1, 24 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 with diethyl ether to give [2-(4-acetamido-phenyl-sulfanyl)-6-(4-hydroxyphenyl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087603B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-8efc810cb17d4a09ab4b16028a84d79f
출처 메모uspto-grants-2006_08