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HRID 1503302作成日:2026年10月26日

Trifluoroacetic acid → 5-bromo-N2-(1,5-dimethyl-1H-pyrazol-4-yl)-N4-methylpyrimidine-2,4-diamine

https://huagongshe.com/reaction/1503302

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物1,5-dimethyl-1H-pyrazol-4-amineHCID 573813—
反応物5-bromo-2-chloro-N-methylpyrimidin-4-amineHCID 10727771—
溶媒2-MethoxyethanolHCID 8019—
生成物5-bromo-N2-(1,5-dimethyl-1H-pyrazol-4-yl)-N4-methylpyrimidine-2,4-diamineHCID 6908193317.1%

反応条件

温度100 °C

反応手順

To a mixture of 5-bromo-2-chloro-N-methylpyrimidin-4-amine (0.201 g, 0.903 mmol) and 1,5-dimethyl-1H-pyrazol-4-amine (0.12 g, 1.08 mmol) in 2-methoxyethanol (2 mL) was added TFA (0.070 mL, 0.9 mmol). The reaction was stirred in a sealed tube at 100° C. for 90 minutes. The resulting precipitate was collected by filtration. The isolated solid was further purified by reverse phase HPLC to give 5-bromo-N2-(1,5-dimethyl-1H-pyrazol-4-yl)-N4-methylpyrimidine-2,4-diamine (46 mg, 17%). LCMS (Method A): [MH+]=297.0 at 2.57 min. 1H-NMR (DMSO): δ 8.28 (s, 1H), 7.84 (s, 1H), 7.49 (s, 1H), 6.79 (d, J=3.4, 1H), 3.67 (s, 3H), 2.82 (d, J=3.6, 3H), 2.14 (s, 3H). Ki=0.017 μM.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09212173B2
出典データセットuspto-grants-2015_12
ORD IDord-83710fec73074483a813934e434f68f9
出典メモuspto-grants-2015_12