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

Triethylamine → HCID 57410108, Verbindung

HRID 527686
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 527686
[CH3:1][C:2]([C:5]([NH:7][C:8]1[CH:13]=[CH:12][C:11]([O:14][C:15]2[C:20]3[C:21]([CH3:24])=[N:22][O:23][C:19]=3[CH:18]=[CH:17][CH:16]=2)=[CH:10][CH:9]=1)=[O:6])([CH3:4])[NH2:3].C(N(CC)CC)C.Cl[C:33](Cl)([O:35]C(=O)OC(Cl)(Cl)Cl)Cl>C(OCC)(=O)C.CN(C1C=CN=CC=1)C>[CH3:4][C:2]1([CH3:1])[NH:3][C:33](=[O:35])[N:7]([C:8]2[CH:13]=[CH:12][C:11]([O:14][C:15]3[C:20]4[C:21]([CH3:24])=[N:22][O:23][C:19]=4[CH:18]=[CH:17][CH:16]=3)=[CH:10][CH:9]=2)[C:5]1=[O:6]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 8471TriethylamineHCID 94429TriphosgeneHCID 67966943HCID 67966943, Verbindung2×

Produkt 1

HCID 57410108HCID 57410108, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 142844-(Dimethylamino)pyridineKatalysator
HCID 8857
Ethyl Acetate
Lösungsmittel
2×

Versuchsvorschrift

2-methyl-N1-{4-[(3-methyl-1,2-benzisoxazol-4-yl)oxy]phenyl}alaninamide (Intermediate 25, 18 mg) was dissolved in 4 ml of ethyl acetate. Triethylamine (0.017 ml, 0.12 mmol) was then added followed by a solution of triphosgene (8.21 mg, 0.028 mmol) in 1.0 ml of ethyl acetate. After stirring for 5 minutes, DMAP (3.4 mg, 0.028 mmol) was added and the reaction mixture was stirred at room temperature for 10 minutes. After quenching with a saturated aqueous solution of NaHCO3, the mixture was extracted two times with ethyl acetate and the collected organic layers were dried over sodium sulphate, filtered and evaporated. The crude obtained was charged on a silica gel column and eluted with c-Hex/EtOAc as eluents (from all 100:0 to 0:100). This afforded 10 mg of the title compound.

Aufarbeitung

  1. stirringthe reaction mixture was stirred at room temperature for 10 minutes
  2. customAfter quenching with a saturated aqueous solution of NaHCO3
  3. extractionthe mixture was extracted two times with ethyl acetate
  4. dry with materialthe collected organic layers were dried over sodium sulphate
  5. filtrationfiltered
  6. customevaporated
  7. customThe crude obtained
  8. additionwas charged on a silica gel column
  9. washeluted with c-Hex/EtOAc as eluents (from all 100:0 to 0:100)

Quellen und Nachweise

ORD-Eintrag
ord-297e26c81ba945ef8353bc70add02aac
Quelldatensatz
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09346790B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion