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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuryl chlorideHCID 24648—
Edukt1-(Prop-2-en-1-yl)cyclopropane-1-sulfonyl chlorideHCID 44181959—
Edukt3,5,6-trifluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamineHCID 59386343—
LösungsmittelPyridineHCID 1049—
Produkt1-Allyl-cyclopropanesulfonic acid [3,4,6-trifluoro-2-(2-fluoro-4-iodo-phenylamino)phenyl]-amideHCID 57626644—

Reaktionsbedingungen

Temperatur40 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09095581B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-182caf2807d84ef799efe0560e10dc7d
Quellennotizuspto-grants-2015_08