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HRID 7612作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物4'-MercaptoacetanilideHCID 70777—
反応物(2-chloro-6-phenyl-pyrimidin-4-yl)-(5-methyl-2H-pyrazol-3-yl)-amineHCID 178418761—
溶媒tert-ButanolHCID 6386—
生成物N-(4-(4-(5-methyl-1H-pyrazol-3-ylamino)-6-phenylpyrimidin-2-ylthio)phenyl)acetamideHCID 17841906185%

反応手順

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%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087603B2
出典データセットuspto-grants-2006_08
ORD IDord-2c9f0fe041d94e3aa4d71ea144b51227
出典メモuspto-grants-2006_08