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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484432Generated: October 26, 2026

N4-Acetylsulfanilamide → HCID 178464663, compound

https://huagongshe.com/reaction/1484432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN4-AcetylsulfanilamideHCID 8482—
ReactantN-ethyl-2,3-diaza-spiro[4.4]non-3-ene-2-carboximidothioic acid methyl esterHCID 53354231—
SolventAcetonitrileHCID 6342—
ProductHCID 178464663HCID 17846466387%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422244B2
Source datasetuspto-grants-2016_08
ORD IDord-95d9982116f6444e8397f412f3ff2ef6
Source noteuspto-grants-2016_08