Potassium Iodide → HCID 20288037, Verbindung

HRID 126870Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 126870
Cl[CH2:2][CH2:3][N:4]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[NH:6][C:5]1=[O:13].Cl.[F:15][C:16]1[CH:21]=[CH:20][C:19]([C:22](=[O:30])[CH2:23][CH:24]2[CH2:29][CH2:28][NH:27][CH2:26][CH2:25]2)=[CH:18][CH:17]=1.C(=O)([O-])[O-].[Na+].[Na+].[I-].[K+]>O.CC(C)CC(=O)C>[F:15][C:16]1[CH:21]=[CH:20][C:19]([C:22](=[O:30])[CH2:23][CH:24]2[CH2:29][CH2:28][N:27]([CH2:2][CH2:3][N:4]3[C:8]4[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=4[NH:6][C:5]3=[O:13])[CH2:26][CH2:25]2)=[CH:18][CH:17]=1

Komponenten

7

Versuchsvorschrift

A mixture of 2.16 parts of 1-(2-chloroethyl)-1,3-dihydro-2H-benzimidazol-2-one, 2.57 parts of 1-(4-fluorophenyl)-2-(4-piperidinyl)ethanone hydrochloride, 5.3 parts of sodium carbonate, 0.2 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone is stirred and refluxed for 15 hours using a water-separator. The reaction mixture is cooled, water is added and the layers are separated. The organic phase is dried, filtered and evaporated. The residue is crystallized from a mixture of 2,2'-oxybispropane and 2-propanol. The product is filtered off and dried, yielding 2.5 parts of 1-[2-[4-[2-(4-fluorophenyl)-2-oxoethyl]-1-piperidinyl]ethyl]-1,3-dihydro-2H-benzimidazol-2-one; mp. 180.6° C.

Aufarbeitung

  1. temperaturerefluxed for 15 hours
  2. temperatureThe reaction mixture is cooled
  3. customthe layers are separated
  4. customThe organic phase is dried
  5. filtrationfiltered
  6. customevaporated
  7. customThe residue is crystallized from a mixture of 2,2'-oxybispropane and 2-propanol
  8. filtrationThe product is filtered off
  9. customdried

Quellen und Nachweise

ORD-Eintrag
ord-173e6664430d41d9ae34feea31fb7027
Quelldatensatz
uspto-grants-1981_03
Patentnummer
US04254127

Notizen zur Reaktion

Wird geladen…