Water → HCID 23368712, Verbindung

HRID 1608849Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1608849
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([NH:17][S:18]([C:21]2[CH:27]=[CH:26][C:24]([CH3:25])=[CH:23][CH:22]=2)(=[O:20])=[O:19])=[C:6]([CH:16]=1)[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[Cl:15])=[O:8].[H-].[Na+].[CH3:30]C(C)(Br)C(N)=O.O.[CH3:38][N:39]([CH:41]=[O:42])[CH3:40]>>[S:18]([N:17]([C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:16][C:6]=1[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[Cl:15])=[O:8])[CH2:30][C:41](=[O:42])[N:39]([CH3:40])[CH3:38])([C:21]1[CH:22]=[CH:23][C:24]([CH3:25])=[CH:26][CH:27]=1)(=[O:19])=[O:20]

Komponenten

6

Edukt 5

HCID 962WaterHCID 6228DimethylformamideHCID 24758Sodium hydrideHCID 1012352-Bromo-2-methylpropanamideHCID 23368680N-[4-Chloro-2-(2-chlorobenzoyl)phenyl]-4-methylbenzene-1-sulfonamide

Produkt 1

HCID 23368712HCID 23368712, Verbindung

Versuchsvorschrift

8.4 g of 5,2'-dichloro-2-tosylaminobenzophenone are dissolved in 40 ml of DMF and treated with 0.7 g of 80% sodium hydride; after 15 minutes, 10 g of dimethylbromoacetamide, prepared in Example 1, are added and the mixture is stirred overnight at RT. The reaction medium is poured into water, the precipitate formed is filtered off and taken up with DCM and the solution is dried and concentrated. 9.2 g of the expected product are obtained after crystallization from isopropyl ether.

Aufarbeitung

  1. additionare added
  2. customthe precipitate formed
  3. filtrationis filtered off
  4. customthe solution is dried
  5. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-bb0243ff86c04b5eb05647f0027c16f2
Quelldatensatz
uspto-grants-1995_03
Patentnummer
US05397801

Notizen zur Reaktion

Wird geladen…