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HCID 22405287, Verbindung → 8-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one

HRID 441222
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 441222
C([O:3][C:4]([CH2:6][CH2:7][NH:8][C:9]1[CH:14]=[CH:13][C:12]([CH3:15])=[CH:11][C:10]=1[N+:16]([O-])=O)=O)C>CO.C(O)(=O)C.[Fe]>[CH3:15][C:12]1[CH:13]=[CH:14][C:9]2[NH:8][CH2:7][CH2:6][C:4](=[O:3])[NH:16][C:10]=2[CH:11]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 1

HCID 22405287HCID 22405287, Verbindung

Produkt 1

HCID 224052058-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-oneAusbeute 16 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 23925IronKatalysatorHCID 176Acetic AcidLösungsmittelHCID 887MethanolLösungsmittel

Versuchsvorschrift

A mixture of N-(2-ethoxycarbonylethyl)-4-methyl-2-nitroaniline (11.25 g) and iron powder (12.45 g) in a mixture of methanol (70 ml) and acetic acid (7 ml) was refluxed for 1 hour and the solution was cooled to ambient temperature. The mixture was filtered through celite and the filtrate was evaporated in vacuo. The residue was dissolved with chloroform (50 ml) and the solution was basified with saturated sodium bicarbonate aqueous solution. The solution was filtered through celite and the organic layer was washed with brine. The solution was dried over magnesium sulfate and the solvent was removed. A mixture of the residue (8.00 g) in a mixture of concentrated hydrochloric acid (16 ml) and water (12 ml) was refluxed for 1 hour and the solution was cooled to ambient temperature. The mixture was basified with concentrated ammonium hydroxide and then the resulting solution was extracted with chloroform. Drying over magnesium sulfate, filtering and the removal of solvents afforded a crude product. The crude product was triturated with diethyl ether - isopropyl ether (1:1) to give 8-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one (1.26 g) as a brown powder.

Aufarbeitung

  1. temperaturewas refluxed for 1 hour
  2. filtrationThe mixture was filtered through celite
  3. customthe filtrate was evaporated in vacuo
  4. dissolutionThe residue was dissolved with chloroform (50 ml)
  5. filtrationThe solution was filtered through celite
  6. washthe organic layer was washed with brine
  7. dry with materialThe solution was dried over magnesium sulfate
  8. customthe solvent was removed
  9. additionA mixture of the residue (8.00 g)
  10. additionin a mixture of concentrated hydrochloric acid (16 ml) and water (12 ml)
  11. temperaturewas refluxed for 1 hour
  12. temperaturethe solution was cooled to ambient temperature
  13. extractionthe resulting solution was extracted with chloroform
  14. dry with materialDrying over magnesium sulfate
  15. filtrationfiltering
  16. customthe removal of solvents
  17. customafforded a crude product
  18. customThe crude product was triturated with diethyl ether - isopropyl ether (1:1)

Quellen und Nachweise

ORD-Eintrag
ord-879d11ac84554005b8862850a9437b3b
Quelldatensatz
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05521170

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