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

Hydrochloric Acid → HCID 23075416, Verbindung

HRID 33601
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 33601
[NH2:1][C:2]1[C:3]([CH3:27])=[C:4]2[C:8](=[C:9]([NH:12][C:13](=[O:18])[C:14]([CH3:17])([CH3:16])[CH3:15])[C:10]=1[CH3:11])[N:7]([CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[CH2:6][CH2:5]2.[Cl:28]S([N:32]=[C:33]=[O:34])(=O)=O.Cl.O>C(Cl)Cl>[ClH:28].[CH3:27][C:3]1[C:2]([NH:1][C:33]([NH2:32])=[O:34])=[C:10]([CH3:11])[C:9]([NH:12][C:13](=[O:18])[C:14]([CH3:16])([CH3:17])[CH3:15])=[C:8]2[C:4]=1[CH2:5][CH2:6][N:7]2[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 70918Chlorosulfonyl isocyanateHCID 23075425N-(5-Amino-4,6-dimethyl-1-octylindolin-7-yl)-2,2-dimethylpropanamide

Produkt 1

HCID 23075416HCID 23075416, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344
Dichloromethane
Lösungsmittel

Versuchsvorschrift

N-(5-Amino-4,6-dimethyl-1-octylindolin-7-yl)-2,2-dimethylpropanamide (500 mg) was dissolved in methylene chloride (5.0 mL), and chlorosulfonyl isocyanate (0.14 mL) was added dropwise at −60° C. The mixture was stirred at the same temperature for 3 hr and 6M hydrochloric acid (0.45 mL) was added. The mixture was stirred at room temperature for 30 min. Water (50 mL) was added to the reaction solution and the mixture was extracted with chloroform (100 mL). The chloroform layer was washed with saturated brine and dried over sodium sulfate. Chloroform was evaporated under reduced pressure and the obtained crystalline residue was recrystallized from a mixture of chloroform-diisopropyl ether to give the title compound as crystals (407 mg).

Aufarbeitung

  1. stirringThe mixture was stirred at room temperature for 30 min
  2. extractionthe mixture was extracted with chloroform (100 mL)
  3. washThe chloroform layer was washed with saturated brine
  4. dry with materialdried over sodium sulfate
  5. customChloroform was evaporated under reduced pressure
  6. customthe obtained crystalline residue was recrystallized from a mixture of chloroform-diisopropyl ether

Quellen und Nachweise

ORD-Eintrag
ord-97faa260617b47e7aceb3f11cb388ad3
Quelldatensatz
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07429612B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion