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HRID 1671769作成日:2026年10月27日

Methylamine → 4-Chloro-N-methyl-6-(4-methylpiperazin-1-yl)-1,3,5-triazin-2-amine

https://huagongshe.com/reaction/1671769

反応式

関与物質

役割名称HCID仕込み量
反応物MethylamineHCID 6329—
反応物Cyanuric chlorideHCID 7954—
反応物Sodium HydroxideHCID 14798—
反応物1-MethylpiperazineHCID 53167—
溶媒Acetonitrile--water (1/1)HCID 18373917—
生成物4-Chloro-N-methyl-6-(4-methylpiperazin-1-yl)-1,3,5-triazin-2-amineHCID 80767500—

反応条件

温度0 °C

反応手順

A mixture of cyanuric chloride (3.86 g, 20.9 mmol, 1 equivalent) in CH3CN/H2O (1/1, 200 ml) was cooled to 0° C. Methylamine solution in water (40% (w), 1.83 ml, 20.9 mmol, 1 equivalent) was added, followed by 1N NaOH (20.9 ml, 20.9 mmol, 1 equivalent). The reaction mixture was stirred at 0° C. for 15 min and LCMS showed the reaction had completed. At 0° C., N-methylpiperazine (2.3 ml, 20.9 mmol, 1 equivalent) was added, followed by 1N NaOH (4.2 ml, 0.2 equivalents). The solution turned to clear. The solvent was evaporated to give the crude product which was further purified with silica gel chromatography (eluant 70% B, solvent B is 10% MeOH in DCM with 1% Et3N) to give the product (1.8 g). 1H NMR (CDCl3, 400 MHz): δ2.33 (s, 3H), 2.44 (br, 4H), 2.95&2.96 (3H), 3.86 (br, 4H), 5.1&5.7 (br, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07994317B2
出典データセットuspto-grants-2011_08
ORD IDord-48a876d6194d42e6a772d7d4ea153860
出典メモuspto-grants-2011_08