StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Sodium hydride → N1-methyl-5-(2-amino-5-cyano-4-pyridyl)oxy-1H-1-indolecarboxamide

HRID 2215592
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2215592
[NH2:1][C:2]1[CH:9]=[C:8]([O:10][C:11]2[CH:12]=[C:13]3[C:17](=[CH:18][CH:19]=2)[NH:16][CH:15]=[CH:14]3)[C:5]([C:6]#[N:7])=[CH:4][N:3]=1.[H-].[Na+].[CH2:22]([NH:25][C:26](=O)[O:27]C1C=CC=CC=1)CC.[Cl-].[NH4+]>CN(C)C=O>[CH3:22][NH:25][C:26]([N:16]1[C:17]2[C:13](=[CH:12][C:11]([O:10][C:8]3[C:5]([C:6]#[N:7])=[CH:4][N:3]=[C:2]([NH2:1])[CH:9]=3)=[CH:19][CH:18]=2)[CH:14]=[CH:15]1)=[O:27]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 11252326Carbamic acid, propyl-, phenyl esterHCID 219493966-Amino-4-(1H-5-indolyloxy)nicotinonitrile

Produkt 1

HCID 21949164N1-methyl-5-(2-amino-5-cyano-4-pyridyl)oxy-1H-1-indolecarboxamideAusbeute 22 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

6-Amino-4-(1H-5-indolyloxy)nicotinonitrile (63 mg, 0.252 mmol) was dissolved in N,N-dimethylformamide (1 ml); and sodium hydride (60% in oil, 11.6 mg, 0.29 mmol) was gradually added thereto while stirring at room temperature. After the reaction mixture was stirred for 30 minutes, phenyl N-propylcarbamate (49.5 mg, 0.277 mmol) was added thereto; and the reaction mixture was stirred for 3 hours. A saturated aqueous solution of ammonium chloride was added thereto; this was subjected to extraction with ethyl acetate, and dried over anhydrous sodium sulfate. This solution was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (Fuji Silysia NH, ethyl acetate-methanol) to yield the title compound (12 mg) and N1-methyl-5-(2-amino-5-cyano-4-pyridyl)oxy-1H-1-indolecarboxamide (17 mg).

Aufarbeitung

  1. stirringAfter the reaction mixture was stirred for 30 minutes
  2. stirringand the reaction mixture was stirred for 3 hours
  3. extractionthis was subjected to extraction with ethyl acetate
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationThis solution was concentrated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (Fuji Silysia NH, ethyl acetate-methanol)

Quellen und Nachweise

ORD-Eintrag
ord-4f29f53f5d304b578ede4e8a88565f5c
Quelldatensatz
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07109219B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion