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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51151생성일: 2026년 10월 24일

2-(Methylsulfonyl)ethanamine → (4-Phenoxyphenyl)-(7-(5-(2-(methanesulphonyl)ethylaminomethyl)furan-2-yl)-quinolin-4-yl)amine

https://huagongshe.com/ko/reaction/51151

반응식

참여 물질

역할이름HCID투입량
반응물2-(Methylsulfonyl)ethanamineHCID 4340561—
반응물5-(4-(4-Phenoxyphenylamino)-quinolin-7-yl)furan-2-carbaldehydeHCID 21951919—
생성물(4-Phenoxyphenyl)-(7-(5-(2-(methanesulphonyl)ethylaminomethyl)furan-2-yl)-quinolin-4-yl)amineHCID 21952211—

반응 단계

5-(4-(4-phenoxyphenylamino)-quinolin-7-yl)furan-2-carbaldehyde (0.05 g) was reacted with 2-(methanesulphonyl)ethylamine (0.075 g) according to procedure D. Acidification with acetic acid (0.5 ml) followed by purification using a ion-exchange (SCX) Bond Elut™ cartridge, eluting with methanol-ammonia (9:1), concentration and trituration with diethylether afforded an off-white solid; δH [2H6]DMSO 8.44 (1H, d), 8.41 (1H, d), 8.11 (1H, s), 7.85 (1H, d), 7.44-7.35 (4H, m), 7.18-7.03 (6H, m), 6.79 (1H, d), 6.47 (1H, d), 3.82 (2H, s), 3.01 (2H, t); m/z 514 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713485B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-50e8e15e152047b0bccb03b0deaa32b8
출처 메모uspto-grants-2004_03