HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724697Generated: October 30, 2026
HCID 21879376, compound → N-2-[4-(1,1-dioxido-3-oxoisothiazolidin-5-yl)phenyl]ethyl-4-phenoxybenzenesulfonamide
https://huagongshe.com/reaction/724697
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 21879376 | HCID 21879376 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | N-2-[4-(1,1-dioxido-3-oxoisothiazolidin-5-yl)phenyl]ethyl-4-phenoxybenzenesulfonamide | HCID 21878675 | 90% |
Reaction Steps
N-2-[4-(2-tert-butyl-1,1-dioxido-3-oxoisothiazolidin-5-yl)phenyl]ethyl-4-phenoxy-benzenesulfonamide (10.0 mg, 0.0184 mmol) was dissolved in trifluoroacetic acid (2 mL). The reaction was heated to 170° C. in the microwave and held at that temperature for 45 seconds. The reaction was chromatographed on a 21.2 mm Luna C18 column using a 20–80% acetonitrile in water gradient with 0.05% trifluoroacetic acid at 25 mL per minute over a 20 minute period. The major fraction was lyophilized to give a white powder (8 mg, 90%). 1H NMR (500 MHz, CD3OD): δ 7.76 (d, J=9.2 Hz, 2H), 7.42 (t, J=7.8 Hz, 2H), 7.37 (d, J=7.8 Hz, 2H), 7.24 (d, J=7.8 Hz, 2H), 7.21 (m, 1H), 7.07 (d, J=7.8 Hz, 2H), 7.03 (d, J=8.8 Hz, 2H), 4.94 (m, 1H), 4.39 (m, 1H), 3.35 (m, 2H), 3.24 (m, 2H), 2.85 (m, 2H); LCMS found for C23H22N2O6S2 (M+H)+: m/z 487.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07141596B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-9c378ddabeba4edba5bf8df7f4f94956 |
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| Source note | uspto-grants-2006_11 |
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