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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1484432Erstellt: 24. Oktober 2026

N4-Acetylsulfanilamide → HCID 178464663, Verbindung

https://huagongshe.com/de/reaction/1484432

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN4-AcetylsulfanilamideHCID 8482—
EduktN-ethyl-2,3-diaza-spiro[4.4]non-3-ene-2-carboximidothioic acid methyl esterHCID 53354231—
LösungsmittelAcetonitrileHCID 6342—
ProduktHCID 178464663HCID 17846466387%

Reaktionsschritte

157 mg (1 mol equiv.) N-Ethyl-2,3-diaza-spiro[4.4]non-3-ene-2-carboximidothioic acid methyl ester and 157 mg (1.05 mol equiv.) 4-acetamidobenzenesulfonamide were taken up in 5 mL acetonitrile. The reaction mixture was refluxed overnight under magnetic stirring and volatiles were removed in vacuo. 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 (ethyl acetate) afforded 236 mg (87%) of N-(4-{[(2,3-diaza-spiro[4.4]non-3-en-2-yl)-ethylamino-methylene]-sulfamoyl}-phenyl)-acetamide. 1H NMR (400 MHz, CDCl3) δ 1.14 (t, J=7.2 Hz, 3H), 1.62-1.83 (m, 8H), 2.20 (s, 3H), 3.43-3.51 (m, 2H), 3.80 (s, 2H), 6.80 (s, 1H), 6.87 (br.s., 1H), 7.56 (d, J=8.8 Hz, 2H), 7.77 (br.s., 1H), 7.83 (d, J=8.8 Hz, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09422244B2
Quelldatensatzuspto-grants-2016_08
ORD IDord-95d9982116f6444e8397f412f3ff2ef6
Quellennotizuspto-grants-2016_08