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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1435160생성일: 2026년 10월 27일

4-Hydrazinobenzenesulfonic acid → 6-(2,3-dimethyl-5-sulfo-3H-indol-3-yl)hexanoic acid

https://huagongshe.com/reaction/1435160

반응식

참여 물질

역할이름HCID투입량
반응물4-Hydrazinobenzenesulfonic acidHCID 66825—
반응물7-Methyl-8-oxononanoic acidHCID 22266823—
용매Acetic AcidHCID 176—
용매Methanol--water (1/1)HCID 22242641—
생성물6-(2,3-dimethyl-5-sulfo-3H-indol-3-yl)hexanoic acidHCID 59855422—

반응 단계

To a stirred solution of 4-hydrazinobenzenesulfonic acid (Aldrich, 11.25 g, 0.06 mol) in acetic acid (50 ml) was added 7-acetyloctanoic acid (16.7 g, 0.09 mol). The reaction mixture was heated under reflux for 12 hrs. Acetic acid was removed under reduced pressure. The resulting solid was dissolved in methanol and reprecipitated with a saturated solution of potassium hydroxide in isopropanol. The solid was filtered, washed with isopropanol and dried, (8 g, 40%). The analytical sample was obtained by C18 reversed phase column chromatography using water/methanol mixture as solvent., m.p. 250° C. dec; IR νcm−1=2930, 2597, and 1719. 1H NMR, D2O, δ, 7.8-7.9 (m, 2H, 4-H and 6-H of aromatic protons); 7.6 (d, J=7 Hz, 1H, 7-H of aromatic); 2.2 (t, J=7 Hz, 2H, —CH2—COOH); 1.9-2.1 (m, 2H, alkyl); 1.2-1.6 (a singlet merged in a multiplet, 7H, —CH3 & (—CH2)2); 0.6-0.9 (m, 2H, alkyl).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07615646B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-7daacfb2ad2947f581353dc1207e0f0a
출처 메모uspto-grants-2009_11