HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840840Generated: October 30, 2026
4-(Methylsulfonyl)aniline → HCID 10911220, compound
https://huagongshe.com/reaction/840840
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Methylsulfonyl)aniline | HCID 79617 | — |
| Reactant | 4-Hydrazinylbenzenesulfonamide hydrochloride | HCID 2794567 | — |
| Reactant | HCID 10911220 | HCID 10911220 | — |
| Product | HCID 10911220 | HCID 10911220 | — |
| Product | HCID 178504651 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06369086B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-4fc21fb6443f4b1ba99d8424b7b12b6b |
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| Source note | uspto-grants-2002_04 |
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