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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7612생성일: 2026년 10월 24일

4'-Mercaptoacetanilide → N-(4-(4-(5-methyl-1H-pyrazol-3-ylamino)-6-phenylpyrimidin-2-ylthio)phenyl)acetamide

https://huagongshe.com/ko/reaction/7612

반응식

참여 물질

역할이름HCID투입량
반응물4'-MercaptoacetanilideHCID 70777—
반응물(2-chloro-6-phenyl-pyrimidin-4-yl)-(5-methyl-2H-pyrazol-3-yl)-amineHCID 178418761—
용매tert-ButanolHCID 6386—
생성물N-(4-(4-(5-methyl-1H-pyrazol-3-ylamino)-6-phenylpyrimidin-2-ylthio)phenyl)acetamideHCID 17841906185%

반응 단계

The above prepared (2-chloro-6-phenyl-pyrimidin-4-yl)-(5-methyl-2H-pyrazol-3-yl)-amine. (60 mg, 0.21 mmol) is combined with 4-acetamidothiophenol (176 mg, 1.05 mmol) in tert-butanol (5 mL) and the mixture heated at reflux for 20 hours. The reaction mixture is cooled to room temperature and partitioned between ethyl acetate and aqueous NaHCO3. The organic layer is washed with brine, dried over MgSO4 and concentrated in vacuo. The resulting residue is purified by flash chromatography (SiO2, DCM/MeOH gradient) to afford [2-(4-acetamido-phenylsulfanyl)-6-phenyl-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine (74 mg, 85%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087603B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-2c9f0fe041d94e3aa4d71ea144b51227
출처 메모uspto-grants-2006_08