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HRID 1621415作成日:2026年10月25日

Water → 4-(2-Chloro-5-methylpyridin-3-yl)-6-methyl-1,3,5-triazin-2-amine

https://huagongshe.com/reaction/1621415

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1,2-DimethoxyethaneHCID 8071—
反応物4-Chloro-6-methyl-1,3,5-triazin-2-amineHCID 30591—
反応物Sodium Carbonate MonohydrateHCID 2735133—
反応物2-Chloro-5-methylpyridine-3-boronic acidHCID 2763126—
触媒HCID 178418397HCID 178418397—
生成物4-(2-Chloro-5-methylpyridin-3-yl)-6-methyl-1,3,5-triazin-2-amineHCID 5954824144.6%

反応条件

温度90 °C

反応手順

A glass microwave reaction vessel was charged with 4-chloro-6-methyl-1,3,5-triazin-2-amine (0.350 g, 2 mmol), 2-chloro-5-methylpyridin-3-ylboronic acid (combi-blocks catalog number BB-3511) (0.6 g, 3 mmol), sodium carbonate, monohydrate, crystal (J. T. Baker catalog number 3600-01) (0.450 g, 7 mmol), tetrakis(triphenylphosphine)palladium (0) (Strem chemicals catalog number 46-Z150) (0.3 g, 0.2 mmol). Degassed 1,2-dimethoxyethane (Aldrich catalog #255527) (11 mL, 109 mmol) and water (1 mL, 2 mmol) were added to the mixture. The reaction mixture was stirred and heated in a Smith Synthesizer® microwave reactor (Personal Chemistry, Inc., Upssala, Sweden) at 90° C. for 30 min. The mixture was filtered through Celite® (diatomaceous earth) and washed with ethyl acetate. The crude product was adsorbed onto a plug of silica gel and chromatographed through a RediSep®, Teledyne ISCO, Lincoln, Nebr., pre-packed silica gel column (40 g), eluting with a gradient of 5% to 10% 2 M NH3/MeOH in dichloromethane, to provide 4-(2-chloro-5-methylpyridin-3-yl)-6-methyl-1,3,5-triazin-2-amine (0.210 g, 36% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08772480B2
出典データセットuspto-grants-2014_07
ORD IDord-f759d95fb8094d7a86829e39f19ec2fb
出典メモuspto-grants-2014_07