Reaktion #52800

ord-249b4bbe4f0c477ca85acdee3086ebaf

Reaktionsgleichung

O=C1Cc2cc(S(=O)(=O)Cl)ccc2N1
5-chlorosulfonyl-2-oxindole
CC(C)N
isopropylamine
c1ccncc1
pyridine
CC(C)NS(=O)(=O)c1ccc2c(c1)CC(=O)N2
5-isopropylaminosulfonyl-2-oxindole
Ausbeute 45.5%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe solid was collected by vacuum filtration
  2. 2
    Waschenslurry-washed with hot ethanol
  3. 3
    Temperaturcooled
  4. 4
    Filtrationcollected by vacuum filtration and vacuum
  5. 5
    Sonstigedried at 40° C.

Vorschrift

A suspension of 3 g of 5-chlorosulfonyl-2-oxindole, 1.15 g of isopropylamine and 1.2 mL of pyridine in 50 mL of dichloromethane was stirred at room temperature for 4 hours at which time a white solid was present. The solid was collected by vacuum filtration, slurry-washed with hot ethanol, cooled, collected by vacuum filtration and vacuum dried at 40° C. to give 1.5 g (45%) of 5-isopropylaminosulfonyl-2-oxindole.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06855730B2uspto-grants-2005_02