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HRID 1095033作成日:2026年10月27日

2-Chloro-5-methylpyrimidin-4-amine → 5-Methyl-N2-(4-(2-(pyrrolidin-1-yl)ethoxy)phenyl)pyrimidine-2,4-diamine

https://huagongshe.com/reaction/1095033

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chloro-5-methylpyrimidin-4-amineHCID 4302175—
反応物4-(2-(Pyrrolidin-1-yl)ethoxy)anilineHCID 6493749—
溶媒Acetic AcidHCID 176—
生成物5-Methyl-N2-(4-(2-(pyrrolidin-1-yl)ethoxy)phenyl)pyrimidine-2,4-diamineHCID 5767508573%

反応手順

A mixture of 2-chloro-5-methyl-pyrimidin-4-ylamine (0.50 g, 3.5 mmol) and 4-(2-pyrrolidin-1-yl-ethoxy)-phenylamine (1.1 g, 5.3 mmol) in acetic acid (8 mL) was sealed in a microwave reaction tube and irradiated with microwave at 150° C. for 15 min. After cooling to room temperature, the cap was removed and the mixture 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 grey solid (0.80 g, 73%). It was used in the next step without purification. MS (ES+): m/z 314 (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-8d6388e6487847ccbfd9896bd0a2692e
出典メモuspto-grants-2012_03