Water → HCID 23364255, Verbindung

HRID 1081496Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1081496
[H-].[Na+].[CH2:3]([O:5][C:6]1[CH:23]=[CH:22][C:9]2[NH:10][C:11](=[O:21])[N:12]([C:13]([CH3:20])([CH3:19])[CH2:14][C:15]([CH3:18])([CH3:17])[CH3:16])[C:8]=2[CH:7]=1)[CH3:4].[CH3:24][O:25][C:26]1[CH:31]=[C:30]([N+:32]([O-:34])=[O:33])[CH:29]=[CH:28][C:27]=1[S:35](Cl)(=[O:37])=[O:36].O>C1COCC1.CN(C=O)C>[CH2:3]([O:5][C:6]1[CH:23]=[CH:22][C:9]2[N:10]([S:35]([C:27]3[CH:28]=[CH:29][C:30]([N+:32]([O-:34])=[O:33])=[CH:31][C:26]=3[O:25][CH3:24])(=[O:36])=[O:37])[C:11](=[O:21])[N:12]([C:13]([CH3:20])([CH3:19])[CH2:14][C:15]([CH3:17])([CH3:16])[CH3:18])[C:8]=2[CH:7]=1)[CH3:4]

Komponenten

7

Versuchsvorschrift

0.2 g of sodium hydride as a 60% dispersion in oil is added in portions to a solution of 1 g of 5-ethoxy-1,3-dihydro-3-(1,1,3,3-tetramethylbutyl)-2H- benzimidazol-2-one in 10 ml of THF and 20 ml of DMF and the mixture is stirred for 30 minutes at RT. 1.2 g of 2-methoxy-4-nitrobenzenesulfonyl chloride are then added and the mixture is stirred for 5 hours at RT. The reaction mixture is poured into 200 ml of water, extracted with AcOEt, washed with water and dried over Na2SO4 and the solvent is evaporated off under vacuum to give 1.1 g of the expected product after crystallization from iso ether. M.p.=158° C.

Aufarbeitung

  1. stirringthe mixture is stirred for 5 hours at RT
  2. extractionextracted with AcOEt
  3. washwashed with water
  4. dry with materialdried over Na2SO4
  5. customthe solvent is evaporated off under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-da824efafad944beb41a84cc2c041117
Quelldatensatz
uspto-grants-1996_12
Patentnummer
US05585394

Notizen zur Reaktion

Wird geladen…