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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840889Generated: October 30, 2026

4-Amino-2-isopropylphenol → HCID 21956235, compound

https://huagongshe.com/reaction/840889

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-2-isopropylphenolHCID 586009—
Reactant4-Hydrazinylbenzenesulfonamide hydrochlorideHCID 2794567—
ReactantHCID 21956235HCID 21956235—
ProductHCID 21956235HCID 21956235—
ProductHCID 178438363HCID 178438363—

Reaction Steps

5-Hydroxy-6-isopropyl-1H-indole-2,3-dione was prepared from 3-isopropyl-4-hydroxyaniline according to Procedure A: 1H NMR (DMSO-d6): δ1.12 (d, J=6.8 Hz, 6H), 3.21 (septet, J=6.9 Hz, 1H), 6.62 (s, 1H), 6.82 (s,1H), 9.51 (1H), 10.61 (s, 1H); ESI−MS m/z 204 (M−H)−. The title compound was prepared from 5-hydroxy-6-isopropyl-1H-indole-2,3-dione and 4-sulfonamidophenylhydrazine hydrochloride according to Procedure G: mp>250° C.; 1H NMR (DMSO-d6): δ1.12 (d, J=7.0 Hz, 6H), 3.21 (septet, J=6.8 Hz, 1H), 6.62 (s, 1H), 6.97 (s, 1H), 7.21 (s, 2H), 7.45 (d, J=8.9 Hz, 2H), 7.75 (d, J=8.7 Hz, 2H), 9.11 (s, 1H), 10.70 (s, 1H), 12.74 (s, 1H); ESI−MS m/z 373 (M−H)−. Anal. Calcd for C17H18N4O4S: C, 54.53; H, 4.85; N, 14.96; S, 8.56. Found: C, 54.37; H, 4.95; N, 14.84; S, 8.48.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369086B1
Source datasetuspto-grants-2002_04
ORD IDord-af5d263031f14a39b0605e86efb8aaab
Source noteuspto-grants-2002_04