Trifluoroacetic acid → 2-Bromo-1-methyl-1H-pyrrole-3-sulfonamide

HRID 2259183

Reaktionsgleichung

Reaktionsgleichung von HRID 2259183
[Br:1][C:2]1[N:3]([CH3:15])[CH:4]=[CH:5][C:6]=1[S:7]([NH:10]C(C)(C)C)(=[O:9])=[O:8].C(O)(C(F)(F)F)=O>C(Cl)Cl>[Br:1][C:2]1[N:3]([CH3:15])[CH:4]=[CH:5][C:6]=1[S:7]([NH2:10])(=[O:8])=[O:9]

Komponenten

4

Edukt 2

HCID 6422Trifluoroacetic acidHCID 196938302-bromo-N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide

Produkt 1

HCID 196938442-Bromo-1-methyl-1H-pyrrole-3-sulfonamideAusbeute 21,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a solution of 7.11 g (24 mmol) of 2-bromo-N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide in 50 mL methylene chloride under a nitrogen atmosphere was added 50 mL of TFA. The reaction mixture was allowed to stir at room temperature overnight ca. 16 hours. The reaction mixture was concentrated in vacuo. Three portions of diethyl ether were added to the crude residue and was removed by evaporation to remove residual TFA, which yielded 1.23 g of the title compound as a light brown solid. 1H NMR (Acetone-d6, 200 MHz.) δ: 7.36(d,1H), 6.49(d,1H), 6.3(bs,2H) 3.68(s,3H).

Aufarbeitung

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. additionThree portions of diethyl ether were added to the crude residue
  3. customwas removed by evaporation
  4. customto remove residual TFA, which

Quellen und Nachweise

ORD-Eintrag
ord-24fca5966e304194948bc21b192c7f7a
Quelldatensatz
uspto-grants-1995_12
Patentnummer
US05472933

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