Phenyl chloroformate → 4-(1,2,3,4,5,6-Hexahydropentalen-1-ylmethyl)-1,3-dihydro-imidazol-2-one

HRID 560069Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 560069
[CH:1]1([CH2:9][C:10]2[N:11]=[CH:12][NH:13][CH:14]=2)[C:8]2[CH2:7][CH2:6][CH2:5][C:4]=2[CH2:3][CH2:2]1.C([O-])(O)=[O:16].[Na+].ClC(OC1C=CC=CC=1)=O>C1COCC1.O>[CH:1]1([CH2:9][C:10]2[NH:11][C:12](=[O:16])[NH:13][CH:14]=2)[C:8]2[CH2:7][CH2:6][CH2:5][C:4]=2[CH2:3][CH2:2]1

Komponenten

6

Edukt 3

HCID 15891Phenyl chloroformateHCID 516892Sodium BicarbonateHCID 178419023HCID 178419023, Verbindung

Produkt 1

HCID 219861944-(1,2,3,4,5,6-Hexahydropentalen-1-ylmethyl)-1,3-dihydro-imidazol-2-one

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittel2×HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A solution of 4-(1,2,3,4,5,6-hexahydro-pentalen-1-ylmethyl)-1H-imidazole; fumarate salt (Intermediate A5 as described in Example A, 340 mg, 1.81 mmol) in THF (15 mL) and water (15 mL) was treated with NaHCO3 (1.52 g, 18 mmol) at rt for 30 m. Phenyl chloroformate (600 mL, 4.7 mmol) was added and stirring was continued for 1 h at 65° C. The mixture was diluted with water (30 mL) and extracted with EtOAc (3×30 mL). The organic portions were combined and freed of solvent. The residue was dissolved in EtOH (15 mL): water (15 mL) and treated with Na2CO3 (500 mg) for 1.5 h at 95° C. The mixture was cooled to rt and the product was collected on a glass frit to give a white solid (˜50%) 4-(1,2,3,4,5,6-Hexahydropentalen-1-ylmethyl)-1,3-dihydro-imidazol-2-one (Compound 41).

Aufarbeitung

  1. extractionextracted with EtOAc (3×30 mL)
  2. dissolutionThe residue was dissolved in EtOH (15 mL)
  3. additionwater (15 mL) and treated with Na2CO3 (500 mg) for 1.5 h at 95° C
  4. customthe product was collected on a glass frit

Quellen und Nachweise

ORD-Eintrag
ord-6f3933ace80642ae9393dfcdf4fea919
Quelldatensatz
uspto-grants-2011_11
Patentnummer
US08063087B2

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