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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 989549생성일: 2026년 10월 24일

Alpha-Cyano-4-Hydroxycinnamic Acid → HCID 178429058, 화합물

https://huagongshe.com/ko/reaction/989549

반응식

참여 물질

역할이름HCID투입량
반응물Alpha-Cyano-4-Hydroxycinnamic AcidHCID 2102—
반응물HCID 178471982HCID 178471982—
생성물HCID 178429058HCID 17842905897%

반응 단계

The title compound was prepared in 97% yield from 3-[5-methyl-3-(2-(N-(2-ethoxycarbonylethyl)-N-benzylaminosulfonyl)phenylsulfonyloxy)phenoxy]propoxyguanidine hydrochloride as prepared in step b of Example 53, in a manner analogous to Example 27. 1H-NMR (300 MHz, DMSO-d6) δ 8.19 (t, J=7.9 Hz, 2H), 7.99 (t, J=7.7 Hz, 1H), 7.88 (t, J=7.8 Hz, 1H), 7.56 (br s, 4H), 7.34 (m, 5H), 6.74 (s, 1H), 6.54 (s, 1H), 6.51 (s, 1H), 4.63 (s, 2H), 3.97 (t, J=6.2 Hz, 2H), 3.89 (t, J=6.1 Hz, 2H), 3.51 (t, J=7.4 Hz, 2H), 2.28 (t, J=7.5 Hz, 4H), 2.22 (s, 3H), 1.99 (pentet, J=6.1 Hz, 2H). Mass spectrun (MALDI-TOF, α-cyano-4-hydroxycinnamic acid matrix) calcd. for C27H32N4O9S2: 621.2 (M+H), 643.2 (M+Na). Found: 621.0, 642.9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06638931B1
출처 데이터셋uspto-grants-2003_10
ORD IDord-05e838591c854a63bc7dd68306246483
출처 메모uspto-grants-2003_10