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HRID 1095035作成日:2026年10月25日

4-(Morpholinomethyl)aniline → 5-Methyl-N2-(4-morpholin-4-ylmethyl-phenyl)-pyrimidine-2,4-diamine

https://huagongshe.com/reaction/1095035

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Morpholinomethyl)anilineHCID 776851—
反応物2-Chloro-5-methylpyrimidin-4-amineHCID 4302175—
溶媒Acetic AcidHCID 176—
生成物5-Methyl-N2-(4-morpholin-4-ylmethyl-phenyl)-pyrimidine-2,4-diamineHCID 5767512483.5%

反応条件

温度70 °C

反応手順

A mixture of 2-chloro-5-methyl-pyrimidin-4-ylamine (0.40 g, 2.8 mmol) and 4-morpholin-4-ylmethyl-phenylamine (0.60 g, 3.1 mmol) in acetic acid (15 mL) was heated at 70° C. for 17 h. After cooling to room temperature, the mixture was concentrated. The residue was taken in water (30 mL) and neutralized with 10% NaOH solution until pH˜10. The resulting aqueous layer was extracted with EtOAc (2×30 mL) and the combined organic layers washed with brine, dried over anhydrous Na2SO4 and filtered. The filtrate was concentrated to afford the title compound as a brown syrup (0.70 g, 83%). It was used in the next step without purification. MS (ES+): m/z 300 (M+H)+

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08133900B2
出典データセットuspto-grants-2012_03
ORD IDord-85f8f3efd8ee4a208fbe796f9b435fbc
出典メモuspto-grants-2012_03