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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14737생성일: 2026년 10월 24일

4-O-Methyldopamine → 2-Methoxy-5-(2-{4-[3-(piperidin-4-ylamino)-phenyl]-pyrimidin-2-ylamino}-ethyl)-phenol

https://huagongshe.com/ko/reaction/14737

반응식

참여 물질

역할이름HCID투입량
반응물4-O-MethyldopamineHCID 1748—
반응물4-[3-(2-Chloro-pyrimidin-4-yl)-phenylamino]-piperidine-1-carboxylic acid tert-butyl esterHCID 86603244—
생성물2-Methoxy-5-(2-{4-[3-(piperidin-4-ylamino)-phenyl]-pyrimidin-2-ylamino}-ethyl)-phenolHCID 58603615—

반응 단계

Intermediate 7 was coupled with 5-(2-Amino-ethyl)-2-methoxy-phenol following procedure F and the resulting product deprotected following procedure G. LC-MS showed the product had the expected M+H+ of 420. 1H NMR (Varian 300 MHz, CD3OD, shifts relative to the solvent peak at 3.3 ppm) δ 8.3 (d, 1H) 7.0-7.6 (m, 8H) 4.95 (m, 1H) 3.89 (m, 1H) 3.7 (m, 1H) 3.4 (m, 2H) 2.9-3.3 (m, 5H) 2.2-2.3 (m, 2H) 1.95 (m, 2H) 1.6-1.8 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732444B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-88f8fb9c568d463580f9acc433714173
출처 메모uspto-grants-2010_06