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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391493Generated: November 3, 2026

Benzenesulfonamide, 3-amino- → HCID 178514716, compound

https://huagongshe.com/reaction/1391493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonamide, 3-amino-HCID 7377—
ReactantHCID 178517101HCID 178517101—
SolventEthanolHCID 702—
ProductHCID 178514716HCID 17851471679.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 0.161 g (1.0 mmol) of (3Z)-3-(hydroxymethylene)-1,3-dihydro-2H-indol-2-one 1,2 and 0.180 g (1.05 mmol) of 3-aminobenzene-1-sulfonamide in 5 ml of EtOH was heated to 80° C. for 45 min. After cooling to ambient temperature, the solid was collected by vacuum filtration and air dried to afford 3-{[(Z)-(2-oxo-1,2-dihydro-3H-indol-3-ylidene)-methyl]amino}benzenesulfonamide as a yellow solid (0.25 g, 79%). mp>250° C.; 1H NMR (DMSO-d6): 6.82 (d, J=7.7 Hz, 1H), 6.87-6.94 (m, 1H), 6.97-7.30 (m, 1H), 7.35 (s, 2H), 7.42-7.47 (m, 1H), 7.50-7.63 (m, 3H), 7.75 (t, J=1.8 Hz, 1H), 8.59 (d, J=12.1 Hz, 1H), 10.53 (s, 1H), 10.85 (d, J=12.3 Hz, 1H); APCI-MS: m/z 316 (m+H)+. Anal. Calcd for C15H13N3O3S: C, 57.13; H, 4.16; N, 13.32; S, 10.17. Found: C, 57.01; H, 4.23; N, 13.30; S, 10.11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07338966B2
Source datasetuspto-grants-2008_03
ORD IDord-d7d067efe55b48089a7dd3bd0bf35d7f
Source noteuspto-grants-2008_03