Sodium hydride → 6-(5-Cyano-2-hydroxy-1H-indol-3-yl)-N-methoxy-N-methylnicotinamide

HRID 1881330Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1881330
[O:1]=[C:2]1[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:11]#[N:12])[CH:8]=2)[NH:3]1.[H-].[Na+].Cl[C:16]1[CH:27]=[CH:26][C:19]([C:20]([N:22]([O:24][CH3:25])[CH3:23])=[O:21])=[CH:18][N:17]=1>CN(C=O)C>[C:11]([C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][CH:6]=1)[NH:3][C:2]([OH:1])=[C:10]2[C:16]1[CH:27]=[CH:26][C:19]([C:20]([N:22]([O:24][CH3:25])[CH3:23])=[O:21])=[CH:18][N:17]=1)#[N:12]

Komponenten

5

Versuchsvorschrift

To a solution of 473 mg (2.99 mmol) of 2-oxoindoline-5-carbonitrile in DMF (10 mL) were added 229 mg (5.73 mmol) of sodium hydride (60% on mineral oil) as a solid. After stirring the resulting suspension for 60 min at RT, a solution of 500 mg (2.49 mmol) of 6-chloro-N-methoxy-N-methylnicotinamide from example 1.1 in DMF (10 mL) was added slowly and the mixture was stirred for 80 min at 120° C. The reaction was cooled down to RT and a saturated solution of NH4CL (40 mL) was added and the resulting precipitate was collected by filtration. The precipitate was washed with water and hexane and afterwards dried in a vacuum oven. Yellow solid. Amount 265 mg. Yield 33%.

Aufarbeitung

  1. stirringthe mixture was stirred for 80 min at 120° C
  2. temperatureThe reaction was cooled down to RT
  3. additiona saturated solution of NH4CL (40 mL) was added
  4. filtrationthe resulting precipitate was collected by filtration
  5. washThe precipitate was washed with water and hexane
  6. customafterwards dried in a vacuum oven

Quellen und Nachweise

ORD-Eintrag
ord-aa1660859cf0460d83d1a426d044d6fa
Quelldatensatz
uspto-grants-2012_11
Patentnummer
US08318793B2

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