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HRID 339795作成日:2026年10月24日

Triethylamine → [1-(4-Methoxyphenyl)ethyl]-2-methylpteridin-4-yl-amine

https://huagongshe.com/ja/reaction/339795

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1,4-Dioxane-2,3-diolHCID 96170—
反応物1-(4-Methoxyphenyl)ethanamineHCID 238181—
反応物6-Chloro-2-methylpyrimidine-4,5-diamineHCID 594145—
溶媒EthanolHCID 702—
溶媒Ethyl acetate hexaneHCID 21226206—
生成物[1-(4-Methoxyphenyl)ethyl]-2-methylpteridin-4-yl-amineHCID 5817422821.3%

反応条件

温度25 °C

反応手順

A mixture of 6-chloro-4,5-diamino-2-methylpyrimidine (317 mg, 2.0 mmol) and 1,4-dioxane-2,3-diol (240 mg, 2.0 mmol) in EtOH (15 mL) was stirred at 25° C. for 1 h. TLC analysis (1:1 hexane/EtOAc on SiO2) indicated complete consumption of starting material. 1-(4-Methoxyphenyl)-ethylamine (332 mg, 2.2 mmol) and triethylamine (Et3N, 0.3 mL, 2.2 mmol) were added, and the reaction was stirred overnight. The majority of solvent was removed in vacuo and the residue was partitioned between EtOAc and H2O. The organic layer was concentrated in vacuo to leave a brown residue that was purified by column chromatography over SiO2, eluting with 2:1 EtOAc/hexane, then 100% EtOAc to afford [1-(4-methoxyphenyl)ethyl]-2-methylpteridin-4-yl-amine (126 mg) as a brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895568B2
出典データセットuspto-grants-2014_11
ORD IDord-f24ae463ec024ff493a47364f93602d2
出典メモuspto-grants-2014_11