HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730210Generated: October 28, 2026
HCID 68949241, compound → HCID 68951993, compound
https://huagongshe.com/reaction/730210
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 68949241 | HCID 68949241 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68951993 | HCID 68951993 | 85.9% |
Reaction Steps
To a solution of the 2-methoxy-N-[2-(4-nitrobenzenesulfonylamino)phenyl]-5-trifluoromethanesulfonylbenzenesulfonamide (1 mmol) in AcOH (5 mL), iron powder (300 mg) was added and the resulting reaction mixture was heated at 100° C. for 30 min. The reaction mixture was filtered through a short pad of Celite and the pad was washed with methanol (50 mL) and dichloromethane (25 mL). The filtrate was concentrated under vacuum. The residue obtained was dissolved in EtOAc (50 mL) and washed with 1% aqueous KOH solution (25 mL). The organic layer was dried over anhydrous sodium sulfate and the solvent was removed to dryness in vacuo to give 486 mg of crude N-[2-(4-aminobenzenesulfonylamino) -phenyl]-2-methoxy-5-trifluoro methanesulfonyl-benzenesulfonamide. LC: Tr 1.09 min; MS: 566.7 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582673B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-26784dd28dd7449cbdbe4ef80b5a52d2 |
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| Source note | uspto-grants-2009_09 |
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