HCID 86637508, Verbindung → 2-Chloro-7,7-difluoro-9-(2-thiophen-2-yl-ethyl)-5,7,8,9-tetrahydro-pyrimido[4,5-b][1,4]diazepin-6-one

HRID 1676801Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1676801
C([O:3][C:4](=O)[C:5]([F:26])([F:25])[CH2:6][N:7]([C:15]1[C:20]([N+:21]([O-])=O)=[CH:19][N:18]=[C:17]([Cl:24])[N:16]=1)[CH2:8][CH2:9][C:10]1[S:11][CH:12]=[CH:13][CH:14]=1)C>C(O)(=O)C.[Fe]>[Cl:24][C:17]1[N:18]=[CH:19][C:20]2[NH:21][C:4](=[O:3])[C:5]([F:26])([F:25])[CH2:6][N:7]([CH2:8][CH2:9][C:10]3[S:11][CH:12]=[CH:13][CH:14]=3)[C:15]=2[N:16]=1

Komponenten

4

Edukt 1

HCID 86637508HCID 86637508, Verbindung

Produkt 1

HCID 866375092-Chloro-7,7-difluoro-9-(2-thiophen-2-yl-ethyl)-5,7,8,9-tetrahydro-pyrimido[4,5-b][1,4]diazepin-6-oneAusbeute 43,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23925IronKatalysatorHCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

To a solution of 1.48 g (0.0035 mole) of 3-[(2-chloro-5-nitro-pyrimidin-4-yl)-(2-thiophen-2-yl-ethyl)-amino]-2,2-difluoro-propionic acid ethyl ester (IV-269) in 20 mL of acetic acid was added 1.5 g (0.027 g-atom) of iron powder. The mixture was heated to 80 degrees for 2 hours and then filtered while hot. Water and ethyl acetate were added to the filtrate and the mixture was stirred for 10 minutes and then filtered. The layers were separated. The organic layer was washed successively with ammonium hydroxide and water, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. Recrystallization of the residue from ethyl acetate and hexane gave 0.52 g of 2-chloro-7,7-difluoro-9-(2-thiophen-2-yl-ethyl)-5,7,8,9-tetrahydro-pyrimido[4,5-b][1,4]diazepin-6-one (VI-269).

Aufarbeitung

  1. temperatureThe mixture was heated to 80 degrees for 2 hours
  2. filtrationfiltered while hot
  3. additionWater and ethyl acetate were added to the filtrate
  4. filtrationfiltered
  5. customThe layers were separated
  6. washThe organic layer was washed successively with ammonium hydroxide and water
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customRecrystallization of the residue from ethyl acetate and hexane

Quellen und Nachweise

ORD-Eintrag
ord-87c3d80eff4f40c8a1661d8f8542b316
Quelldatensatz
uspto-grants-2011_08
Patentnummer
US08003785B2

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