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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14714생성일: 2026년 10월 23일

Phenethylamine → N-(3-Amino-propyl)-N-[3-(2-phenethylamino-pyrimidin-4-yl)-benzyl]methanesulfonamide

https://huagongshe.com/ko/reaction/14714

반응식

참여 물질

역할이름HCID투입량
반응물PhenethylamineHCID 1001—
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-phenethylamino-pyrimidin-4-yl)-benzyl]methanesulfonamideHCID 58603522—

반응 단계

Intermediate 4 was coupled to phenethylamine following procedure F and the resulting product deprotected following procedure G. LC-MS showed the product had the expected M+H+ of 440. 1H NMR (Varian 300 MHz, CDCl3—CD3OD, shifts relative to the solvent peak at 7.24 ppm) δ 8.1 (m, 3H) 7.7 (m, 1H) 7.5 (m, 2H) 7.2 (m, 5H) 4.5 (d, 2H) 3.8 (m, 2H) 3.6 (m, 1H) 3.3 (m, 3H) 3.0 (m, 2H) 2.9 (s, 3H) 1.8 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732444B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-58b0ae1c22044c869bd387b72df5a754
출처 메모uspto-grants-2010_06