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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1484465생성일: 2026년 10월 25일

1H-Indole-5-sulfonamide → HCID 178464642, 화합물

https://huagongshe.com/reaction/1484465

반응식

참여 물질

역할이름HCID투입량
반응물1H-Indole-5-sulfonamideHCID 21683100—
반응물N-ethyl-2,3-diaza-spiro[4.4]non-3-ene-2-carboximidothioic acid methyl esterHCID 53354231—
용매AcetonitrileHCID 6342—
생성물HCID 178464642HCID 17846464287%

반응 단계

100 mg (1 mol equiv.) N-Ethyl-2,3-diaza-spiro[4.4]non-3-ene-2-carboximidothioic acid methyl ester and 92.5 mg (1.05 mol equiv.) 1H-indole-5-sulfonic acid amide were added to 3 mL acetonitrile. The reaction mixture was refluxed overnight and volatiles were removed under reduced pressure. The residue was taken up in ethyl acetate and extracted with 2N NaOH. The organic layer was dried over Na2SO4, filtered and evaporated to dryness. Purification by flash chromatography on silica gel (Et2O:EtOAc=1:1) afforded 152 mg (87%) 1H-indole-5-sulfonic acid (2,3-diaza-spiro[4.4]non-3-en-2-yl)-ethylamino-methyleneamide. 1H NMR (400 MHz, CDCl3) δ 1.14 (t, J=7.2 Hz, 3H), 1.59-1.79 (m, 8H), 3.43-3.51 (m, 2H), 3.79 (br.s., 2H), 6.63-6.65 (m, 1H), 6.76 (s, 1H), 6.99 (br.s., 1H), 7.30 (t, J=2.8 Hz, 1H), 7.43 (d, J=8.6 Hz, 1H), 7.76 (dd, J=8.6, 1.8 Hz, 1H), 8.27 (br.s., 1H), 8.54 (br.s., 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09422244B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-8a2f8b2419a246669fe99ede3e634c33
출처 메모uspto-grants-2016_08