HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 508143Erstellt: 24. Oktober 2026
Sulfuryl chloride → 1-Allyl-cyclopropanesulfonic acid [3,4,6-trifluoro-2-(2-fluoro-4-iodo-phenylamino)phenyl]-amide
https://huagongshe.com/de/reaction/508143
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sulfuryl chloride | HCID 24648 | — |
| Edukt | 1-(Prop-2-en-1-yl)cyclopropane-1-sulfonyl chloride | HCID 44181959 | — |
| Edukt | 3,5,6-trifluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine | HCID 59386343 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | 1-Allyl-cyclopropanesulfonic acid [3,4,6-trifluoro-2-(2-fluoro-4-iodo-phenylamino)phenyl]-amide | HCID 57626644 | — |
Reaktionsschritte
To a stirred solution of the amine, i.e., 3,5,6-trifluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine, (1 eq) in anhydrous pyridine (5 ml/mmole) was added the sulfonyl chloride, i.e., 1-allyl-cyclopropanesulfonyl chloride, (1-5 eq). The reaction mixture was stirred at 40° C. for 48 hours. The reaction mixture was partitioned with water and EtOAc. The organic layer was washed with brine, dried (MGSO4) and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica. 1H NMR (CDCl3, 300 MHz): δ 7.41 (dd, 1H), 7.38 (dd, 1H), 7.09 (s, 1H), 6.78 (m, 1H), 6.49 (m, 1H), 5.96 (s, 1H), 5.86 (m, 1H), 5.18 (d, 2H), 2.76 (d, 2H), 1.23 (m, 2H), 0.872 (m, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09095581B2 |
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| Quelldatensatz | uspto-grants-2015_08 |
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| ORD ID | ord-182caf2807d84ef799efe0560e10dc7d |
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| Quellennotiz | uspto-grants-2015_08 |
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