Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263984Generated: October 26, 2026

Sulfanilamide → 3-(1-Dimethylaminoethylidene)-5-(oxazol-5-yl)-1,3-dihydroindol-2-one

https://huagongshe.com/reaction/1263984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfanilamideHCID 5333—
Reactant1,1-Dimethoxyethyl(dimethyl)amineHCID 87835—
Reactant5-(Oxazol-5-yl)-1,3-dihydroindol-2-oneHCID 11008941—
Reactant3-(1-Dimethylaminoethylidene)-5-(oxazol-5-yl)-1,3-dihydroindol-2-oneHCID 57184042—
Product3-(1-Dimethylaminoethylidene)-5-(oxazol-5-yl)-1,3-dihydroindol-2-oneHCID 57184042—
Product4-[1-[5-(1,3-oxazol-5-yl)-2-oxo-1H-indol-3-ylidene]ethylamino]benzenesulfonamideHCID 178463326—

Reaction Steps

3-(1-Dimethylaminoethylidene)-5-(oxazol-5-yl)-1,3-dihydroindol-2-one was prepared from 5-(oxazol-5-yl)-1,3-dihydroindol-2-one and N,N-dimethylacetamide dimethyl acetal according to Procedure H. Condensation of 3-(1-dimethylaminoethylidene)-5-(oxazol-5-yl)- 1,3-dihydroindol-2-one and sulfanilamide according to Procedure J provided the title compound: mp>250° C.; 1H NMR (DMSO-d6): δ 2.51 (s, 0.8H, DMSO), 2.61 (s, 3H), 6.97 (d, J=8.2 Hz, 1H), 7.37 (s, 2H), 7.40 (dd, J=8.0, 1.5 Hz, 1H), 7.45 (d, J=8.8 Hz, 2H), 7.56 (s, 1H), 7.66 (d, J=1.2 Hz, 1H), 7.83 (d, J=8.5 Hz, 2H), 8.34 (s, 1H), 10.85 (s, 1H), 12.33 (s, 1H); APCI−MS m/z 395 (M−H)−. Anal. Calcd for C19H16N4O4S.0.1 C2H6OS.0.6 H2O: C, 55.56; H, 4.32; N, 13.50; S, 8.50. Found: C, 55.53; H, 4.32; N, 13.27; S. 8.58.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541503B2
Source datasetuspto-grants-2003_04
ORD IDord-16f47676429f4278b7825d5ceebcb959
Source noteuspto-grants-2003_04