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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51148생성일: 2026년 10월 24일

2-(Methylsulfonyl)ethanamine → N-(4-(3-(trifluoromethyl)benzyloxy)phenyl)-6-(5-((2-(methylsulfonyl)ethylamino)methyl)furan-2-yl)quinazolin-4-amine

https://huagongshe.com/ko/reaction/51148

반응식

참여 물질

역할이름HCID투입량
반응물2-(Methylsulfonyl)ethanamineHCID 4340561—
반응물5-(4-{4-(3-Trifluoromethylbenzyloxy)anilino}-6-quinazolinyl)-furan-2-carbaldehydeHCID 21952269—
생성물N-(4-(3-(trifluoromethyl)benzyloxy)phenyl)-6-(5-((2-(methylsulfonyl)ethylamino)methyl)furan-2-yl)quinazolin-4-amineHCID 9808725—

반응 단계

Prepared according to Procedure D from 5-(4-{4-(3-trifluoromethylbenzyloxy)anilino}-6-quinazolinyl)-furan-2-carbaldehyde (0.6 equiv) and 2-methanesulphonyl-ethylamine (1 equiv). 1H NMR 300 MHz (DMSO-d6) 11.63 (bs, 1H); 9.88 (bs, 1H); 9.59 (bs, 1H); 8.88 (s, 1H); 8.43 (d, 1H); 7.97 (d, 1H); 7.90-7.67 (m, 6H); 7.34 (d, 1H); 7.19 (d, 2H); 6.89 (d, 1H); 5.30 (s, 2H); 4.45 (s, 2H); 3. 78 (m, 2H); 3.45 (m, 2H, obscured by water peak); 3.19 (s, 3H); MS m/z 597 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713485B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-d2bfad2d906b4fe9af09cb34efef75cf
출처 메모uspto-grants-2004_03