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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14720생성일: 2026년 10월 24일

p-Methylphenethylamine → N-(3-Amino-propyl)-N-{3-[2-(2-p-tolyl-ethylamino)-pyrimidin-4-yl]-benzyl}-methanesulfonamide

https://huagongshe.com/ko/reaction/14720

반응식

참여 물질

역할이름HCID투입량
반응물p-MethylphenethylamineHCID 76751—
반응물(3-{[3-(2-Chloro-pyrimidin-4-yl)-benzyl]-methanesulfonyl-amino}-propyl)-carbamic acid tert-butyl esterHCID 86603242—
생성물N-(3-Amino-propyl)-N-{3-[2-(2-p-tolyl-ethylamino)-pyrimidin-4-yl]-benzyl}-methanesulfonamideHCID 58603728—

반응 단계

Intermediate 4 was coupled to 2-p-tolyl-ethylamine following procedure F and the resulting product deprotected following procedure G. LC-MS showed the product had the expected M+H+ of 454. 1H NMR (Varian 300 MHz, CDCl3, shifts relative to the solvent peak at 7.24 ppm) δ 9.55 (br s, 1H) 8.1 (m, 2H) 7.6 (m, 4H) 7.2 (m, 4H) 4.4 (s, 2H) 3.81 (s, 2H) 3.37 (m, 2H) 2.97 (m, 4H) 2.94 (s, 3H) 2.25 (s, 3H) 1.75 (s, 2H) 1.69 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732444B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-97e838f45c2247fbaa9cd15fba817f7d
출처 메모uspto-grants-2010_06