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HRID 41364作成日:2026年10月23日

2,4,6-Trimethylaniline → 5-bromo-2-chloro-N-(2,4,6-trimethylphenyl)-4-pyrimidinamine

https://huagongshe.com/ja/reaction/41364

反応式

関与物質

役割名称HCID仕込み量
反応物2,4,6-TrimethylanilineHCID 6913—
反応物DiisopropylethylamineHCID 81531—
反応物5-Bromo-2,4-dichloropyrimidineHCID 289973—
溶媒1,4-DioxaneHCID 31275—
生成物5-bromo-2-chloro-N-(2,4,6-trimethylphenyl)-4-pyrimidinamineHCID 2217008665%
生成物5-bromo4-chloro-N-(2,4,6-trimethylphenyl)-2-pyrimidinamineHCID 2217010224%

反応手順

Reaction under argon atmosphere. A solution of 2,4,6-trimethylbenzenamine (0.00461 mol) in 1,4-dioxane (5 ml) was added to a solution of 5-bromo-2,4-dichloropyrimidine (0.00439 mol) in 1,4-dioxane (5 ml). N,N-bis(1-methylethyl)ethanamine (0.00548 mol) was added. The reaction mixture was stirred and refluxed for 20 hours. The solvent was evaporated. The residue was dissolved in ethyl acetate, washed with a saturated aqueous sodium bicarbonate solution, water and brine, dried with sodium sulfate, filtered, and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: 1:5, 1:2 and 1:1 CH2Cl2:hexane). Two pure fraction groups were collected and their solvent was evaporated, yielding 0.35 g (24%) of 5-bromo-4-chloro-N-(2,4,6-trimethylphenyl)-2-pyrimidinamine (interm. 1) and 0.93 g (65%) of 5-bromo-2-chloro-N-(2,4,6-trimethylphenyl)-4-pyrimidinamine (interim 2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530655B2
出典データセットuspto-grants-2013_09
ORD IDord-3bb703817bf14abc9d6d994f0b8ceef3
出典メモuspto-grants-2013_09