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HRID 1746704作成日:2026年10月27日

N-Methylcyclohexylamine → 6-(cyclohexyl(methyl)amino)-N-(4-hydroxyphenyl)pyrimidine-4-carboxamide

https://huagongshe.com/reaction/1746704

反応式

関与物質

役割名称HCID仕込み量
反応物N-MethylcyclohexylamineHCID 7514—
反応物TriethylamineHCID 8471—
反応物6-chloro-N-(4-hydroxy-2-methylphenyl)pyrimidine-4-carboxamideHCID 59447105—
溶媒TetrahydrofuranHCID 8028—
生成物6-(cyclohexyl(methyl)amino)-N-(4-hydroxyphenyl)pyrimidine-4-carboxamideHCID 25182758—

反応手順

A solution of 6-chloro-N-(4-hydroxy-2-methylphenyl)pyrimidine-4-carboxamide, Intermediate 7 (75.0 mg; 0.30 mmol) in THF (4 mL) was treated with triethylamine (42 μl; 0.30 mmol) and N-methylcyclohexylamine (Aldrich, 43 μl; 0.33 mmol). The reaction mixture was stirred for 24 h. The solvents were removed in vacuo, then the crude product was purified by column chromatography (silica), eluting with cyclohexane containing an increasing amount of EtOAc. The title compound was obtained as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09150519B2
出典データセットuspto-grants-2015_10
ORD IDord-5cbaae8696f74418969f2a1775b820da
出典メモuspto-grants-2015_10