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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1255884생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1255884

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1,4-Dioxane-2,3-diolHCID 96170—
반응물1-(4-Methoxyphenyl)ethanamineHCID 238181—
반응물6-Chloro-2-methylpyrimidine-4,5-diamineHCID 594145—
용매EthanolHCID 702—
용매Ethyl acetate hexaneHCID 21226206—
생성물[1-(4-Methoxyphenyl)ethyl]-2-methylpteridin-4-yl-amineHCID 5817422821.3%

반응 조건

온도25 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08461164B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-2d652c990f454b36b30dbadce40fb6c8
출처 메모uspto-grants-2013_06