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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840840Generated: October 30, 2026

4-(Methylsulfonyl)aniline → HCID 10911220, compound

https://huagongshe.com/reaction/840840

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Methylsulfonyl)anilineHCID 79617—
Reactant4-Hydrazinylbenzenesulfonamide hydrochlorideHCID 2794567—
ReactantHCID 10911220HCID 10911220—
ProductHCID 10911220HCID 10911220—
ProductHCID 178504651HCID 178504651—

Reaction Steps

5-Methylsulfonyl-1H-indole-2,3-dione was prepared from 4-methylsulfonylaniline according to Procedure A: 1H NMR (DMSO-d6): δ3.21 (s, 3H), 7.07(d, J=8.3 Hz, 1H), 7.92 (d, J=1.7 Hz, 1H), 8.05 (dd, J=8.2, 2.0 Hz, 1H), 11.46 (s, 1H); APCI−MS m/z 225 (M)−. The title compound was prepared from 5-methylsulfonyl-1H-indole-2,3-dione and 4-sulfonamidophenylhydrazine hydrochloride according to Procedure G: mp>250° C.; 1H NMR (DMSO-d6): δ3.20 (s, 3H), 7.11 (d, J=8.3 Hz, 1H), 7.26 (s, 2H), 7.65 (d, J=8.9 Hz, 2H), 7.78 (d, J=8.7 Hz, 2H), 7.79 (dd, J=8.2, 1.9 Hz, 1H), 8.06 (d, J=1.6 Hz, 1H), 11.54 (s, 1H), 12.75 (s, 1H); APCI−MS m/z 394 (M)−. Anal. Calcd for C15H14N4O5S2.0.9H2O: C, 43.87; H, 3.88; N, 13.64; S, 15.62. Found: C, 43.96; H, 3.80; N, 13.58; S, 15.67.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369086B1
Source datasetuspto-grants-2002_04
ORD IDord-4fc21fb6443f4b1ba99d8424b7b12b6b
Source noteuspto-grants-2002_04