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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1671769생성일: 2026년 10월 26일

Methylamine → 4-Chloro-N-methyl-6-(4-methylpiperazin-1-yl)-1,3,5-triazin-2-amine

https://huagongshe.com/reaction/1671769

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참여 물질

역할이름HCID투입량
반응물MethylamineHCID 6329—
반응물Cyanuric chlorideHCID 7954—
반응물Sodium HydroxideHCID 14798—
반응물1-MethylpiperazineHCID 53167—
용매Acetonitrile--water (1/1)HCID 18373917—
생성물4-Chloro-N-methyl-6-(4-methylpiperazin-1-yl)-1,3,5-triazin-2-amineHCID 80767500—

반응 조건

온도0 °C

반응 단계

A mixture of cyanuric chloride (3.86 g, 20.9 mmol, 1 equivalent) in CH3CN/H2O (1/1, 200 ml) was cooled to 0° C. Methylamine solution in water (40% (w), 1.83 ml, 20.9 mmol, 1 equivalent) was added, followed by 1N NaOH (20.9 ml, 20.9 mmol, 1 equivalent). The reaction mixture was stirred at 0° C. for 15 min and LCMS showed the reaction had completed. At 0° C., N-methylpiperazine (2.3 ml, 20.9 mmol, 1 equivalent) was added, followed by 1N NaOH (4.2 ml, 0.2 equivalents). The solution turned to clear. The solvent was evaporated to give the crude product which was further purified with silica gel chromatography (eluant 70% B, solvent B is 10% MeOH in DCM with 1% Et3N) to give the product (1.8 g). 1H NMR (CDCl3, 400 MHz): δ2.33 (s, 3H), 2.44 (br, 4H), 2.95&2.96 (3H), 3.86 (br, 4H), 5.1&5.7 (br, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07994317B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-48a876d6194d42e6a772d7d4ea153860
출처 메모uspto-grants-2011_08