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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1845생성일: 2026년 10월 24일

1-Methylpiperazine → 5-Fluoro-2-(4-fluorobenzyl)-4-(4-methylpiperazin-1-yl)-pyrimidine

https://huagongshe.com/ko/reaction/1845

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylpiperazineHCID 53167—
반응물4-Chloro-5-fluoro-2-(4-fluorobenzyl)-pyrimidineHCID 19691354—
용매DichloromethaneHCID 6344—
생성물5-Fluoro-2-(4-fluorobenzyl)-4-(4-methylpiperazin-1-yl)-pyrimidineHCID 1969126496.9%

반응 단계

A mixture of 0.48 g (2 mmol) of 4-chloro-5-fluoro-2-(4-fluorobenzyl)-pyrimidine from Step 2 and 1.53 mL (14 mmol) of 4-methylpiperazine in 10 mL of methylene chloride was stirred at ambient temperature for 1.5 hours. The reaction mixture was concentrated in vacuo and the residue was dissolved in methylene chloride. The resultant solution was washed with 4 X 30 mL of water, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to give 0.59 g (95% yield) of the title compound as an oil; 1H NMR (CDCl3) d 2.32 (s, 3H), 2.47 (t, 4H), 3.78 (t, 4H), 3.99 (s, 2H), 6.97 (m, 2H), 7.29 (m, 2H), 7.97 (d, 1H). The product was carried on to the next step without purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726182
출처 데이터셋uspto-grants-1998_03
ORD IDord-9f9fb1d3a7e54201b973e3a877894221
출처 메모uspto-grants-1998_03