Potassium Iodide → DES(6-fluoro-1,2-benzoxazole)-2,4-difluorobenzoyl risperidone

HRID 969735

Reaktionsgleichung

Reaktionsgleichung von HRID 969735
Cl.[F:2][C:3]1[CH:16]=[C:15]([F:17])[CH:14]=[CH:13][C:4]=1[C:5]([CH:7]1[CH2:12][CH2:11][NH:10][CH2:9][CH2:8]1)=[O:6].Cl[CH2:19][CH2:20][C:21]1[C:26](=[O:27])[N:25]2[CH2:28][CH2:29][CH2:30][CH2:31][C:24]2=[N:23][C:22]=1[CH3:32].C(=O)([O-])O.[Na+].[I-].[K+]>O.C(#N)C>[F:2][C:3]1[CH:16]=[C:15]([F:17])[CH:14]=[CH:13][C:4]=1[C:5]([CH:7]1[CH2:8][CH2:9][N:10]([CH2:19][CH2:20][C:21]2[C:26](=[O:27])[N:25]3[CH2:28][CH2:29][CH2:30][CH2:31][C:24]3=[N:23][C:22]=2[CH3:32])[CH2:11][CH2:12]1)=[O:6]

Komponenten

7

Versuchsvorschrift

A suspension of 29.2 g (0.1116 mole) of 4-(2,4-difluoro-benzoyl)-piperidine-hydrochloride, 25.3 g (0.1117 mole) of 3-(2-chloroethyl)-6,7,8,9-tetrahydro-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one, 500 ml of acetonitrile, 19.6 g (0.2333 mole) of sodium hydrogencarbonate and 0.25 g (0.0015 mole) of potassium iodide is heated to boiling for 10 hours with stirring. The reaction mixture is cooled to room temperature, to the residue 200 ml of water are added. The mixture is stirred for 30 minutes and extracted with 200 ml of dichloromethane. The organic phase is separated, dried over magnesium sulfate, filtered and the filtrate is evaporated. The oily residue thus obtained is purified as follows:

Aufarbeitung

  1. temperatureis heated
  2. additionare added
  3. stirringThe mixture is stirred for 30 minutes
  4. extractionextracted with 200 ml of dichloromethane
  5. customThe organic phase is separated
  6. dry with materialdried over magnesium sulfate
  7. filtrationfiltered
  8. customthe filtrate is evaporated
  9. customThe oily residue thus obtained
  10. customis purified

Quellen und Nachweise

ORD-Eintrag
ord-12fc39fc25a4411fbc84b164281c31d8
Quelldatensatz
uspto-grants-2007_12
Patentnummer
US07307168B2

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