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HRID 1937416作成日:2026年10月27日

2-Chloro-N,N-dimethylpyrimidin-4-amine → N4,N4-dimethyl-N2-[1-(2-phenylethyl)-4-piperidinyl]-2,4-pyrimidinediamine

https://huagongshe.com/reaction/1937416

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chloro-N,N-dimethylpyrimidin-4-amineHCID 95975—
反応物1-(2-Phenylethyl)piperidin-4-amineHCID 10728788—
溶媒WaterHCID 962—
生成物N4,N4-dimethyl-N2-[1-(2-phenylethyl)-4-piperidinyl]-2,4-pyrimidinediamineHCID 5392113128.4%

反応条件

温度120 °C

反応手順

A mixture of 1-(2-phenylethyl)-4-piperidinamine (8.17 g) and 2-chloro-N,N-dimethyl-4-pyrimidinamine (6.3 g) was stirred for 20 hours at 120° C. The reaction mixture was diluted with water and extracted with CH2Cl2. The organic layer was washed with water, dried, filtered and the solvent evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH(NH3) 96/4). The pure fractions were collected and the solvent evaporated. The residue was crystallized from CH3CN. The precipitate was filtered off and dried, yielding 3.69 g (28.4%) of N4,N4-dimethyl-N2-[1-(2-phenylethyl)-4-piperidinyl]-2,4-pyrimidinediamine (comp. 11).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06395742B1
出典データセットuspto-grants-2002_05
ORD IDord-58cd85450cae421b8d8e48d75748ed99
出典メモuspto-grants-2002_05