Potassium Iodide → HCID 13078406, Verbindung

HRID 223260

Reaktionsgleichung

Reaktionsgleichung von HRID 223260
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][N:8]=[C:7]([CH:10]3[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]3)[C:6]=2[CH:16]=1.Cl[CH2:18][CH2:19][CH2:20][N:21]1[C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][C:24]=2[NH:23][C:22]1=[O:30].C(=O)([O-])[O-].[Na+].[Na+].[I-].[K+]>CC(CC(=O)C)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][N:8]=[C:7]([CH:10]3[CH2:11][CH2:12][N:13]([CH2:18][CH2:19][CH2:20][N:21]4[C:25]5[CH:26]=[CH:27][CH:28]=[CH:29][C:24]=5[NH:23][C:22]4=[O:30])[CH2:14][CH2:15]3)[C:6]=2[CH:16]=1

Komponenten

6

Versuchsvorschrift

A mixture of 3.9 g of 5-fluoro-3-(4-piperidyl)-1,2-benzisoxazole, 3.8 g of 1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one, 2.7 g of sodium carbonate, a few crystals of potassium iodide and 140 ml of 2-methyl-4-pentanone was stirred and was heated under reflux under nitrogen for 8 hrs. After stirring at ambient temperature for 12 hrs, the mixture was filtered and the filter cake was stirred with 200 ml of water. The solid was collected and dried. Recrystallization from methanol-dimethylformamide-water gave 2.5 g (35.8%) of product. The product was combined with 1.0 g of that from another run to yield a total of 3.5 g of product, mp 202°-204°.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureunder reflux under nitrogen for 8 hrs
  3. filtrationthe mixture was filtered
  4. stirringthe filter cake was stirred with 200 ml of water
  5. customThe solid was collected
  6. customdried
  7. customRecrystallization from methanol-dimethylformamide-water

Quellen und Nachweise

ORD-Eintrag
ord-8e1307a36c514b7da7d1b2f7684cdf0d
Quelldatensatz
uspto-grants-1982_10
Patentnummer
US04352811

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