Potassium Carbonate → Tert-butyl {4-[(3-amino-7-bromoquinolin-4-ylamino)methyl]benzyl}carbamate

HRID 9490

Reaktionsgleichung

Reaktionsgleichung von HRID 9490
C(=O)([O-])[O-].[K+].[K+].S(S([O-])=O)([O-])=O.[Na+].[Na+].[C:15]([O:19][C:20](=[O:45])[NH:21][CH2:22][C:23]1[CH:28]=[CH:27][C:26]([CH2:29][NH:30][C:31]2[C:40]3[C:35](=[CH:36][C:37]([Br:41])=[CH:38][CH:39]=3)[N:34]=[CH:33][C:32]=2[N+:42]([O-])=O)=[CH:25][CH:24]=1)([CH3:18])([CH3:17])[CH3:16]>O.ClCCl.CC[N+]1C=CC(C2C=C[N+](CC)=CC=2)=CC=1.[Br-].[Br-]>[C:15]([O:19][C:20](=[O:45])[NH:21][CH2:22][C:23]1[CH:28]=[CH:27][C:26]([CH2:29][NH:30][C:31]2[C:40]3[C:35](=[CH:36][C:37]([Br:41])=[CH:38][CH:39]=3)[N:34]=[CH:33][C:32]=2[NH2:42])=[CH:25][CH:24]=1)([CH3:18])([CH3:16])[CH3:17]

Komponenten

7

Edukt 3

HCID 11430Potassium CarbonateHCID 24489Sodium DithioniteHCID 21984421Tert-butyl {4-[(7-bromo-3-nitroquinolin-4-ylamino)methyl]benzyl}carbamate

Produkt 1

HCID 21984367Tert-butyl {4-[(3-amino-7-bromoquinolin-4-ylamino)methyl]benzyl}carbamateAusbeute 100,5 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 114742621,1'-Diethyl-4,4'-bipyridinium dibromideKatalysatorHCID 962WaterLösungsmittel3×HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

Ethyl viologen dibromide (0.069 g, 0.18 mmol), potassium carbonate (12.76 g, 92 mmol) in water (55mL), and sodium hydrosulfite (11.25 g, 65 mmol) in water (55mL) were added sequentially to a solution of tert-butyl{4-[(7-bromo-3-nitroquinolin-4-ylamino)methyl]benzyl}carbamate (9.0 g, 18.5 mmol) in dichloromethane (110 mL). The resulting biphasic mixture was stirred for 20 hours. The reaction was diluted with water (600 mL) and dichloromethane (500 mL). The layers were separated and the aqueous fraction was extracted with dichloromethane. The organic fractions were combined and washed sequentially with water and saturated aqueous sodium chloride. The organic fraction was dried over sodium sulfate, filtered, and concentrated under reduced pressure to yield 8.5 g of tert-butyl{4-[(3-amino-7-bromoquinolin-4-ylamino)methyl]benzyl}carbamate as a yellow-brown amorphous solid.

Aufarbeitung

  1. customThe layers were separated
  2. extractionthe aqueous fraction was extracted with dichloromethane
  3. washwashed sequentially with water and saturated aqueous sodium chloride
  4. dry with materialThe organic fraction was dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-e14b4f690e7d423e92497dc07775b581
Quelldatensatz
uspto-grants-2006_08
Patentnummer
US07091214B2

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