Potassium Iodide → HCID 13319848, compound

HRID 280880Notes

Reaction equation

HRID 280880 reaction equation
Cl[CH2:2][CH2:3][CH2:4][C:5]1[C:9]2[CH:10]=[CH:11][C:12]([F:14])=[CH:13][C:8]=2[O:7][N:6]=1.[NH:15]1[CH2:19][CH2:18][CH2:17][CH2:16]1.[C:20](=[O:23])([OH:22])[O-].[Na+].[I-].[K+].CN(C)C=[O:30]>>[C:8]([OH:7])(=[O:30])[C:20]([OH:22])=[O:23].[F:14][C:12]1[CH:11]=[CH:10][C:9]2[C:5]([CH2:4][CH2:3][CH2:2][N:15]3[CH2:19][CH2:18][CH2:17][CH2:16]3)=[N:6][O:7][C:8]=2[CH:13]=1

Participants

6

Conditions

Temperature
70 °C

Procedure

To 50 ml of dry dimethylformamide, was added 4.2 g of 3-(3-chloropropyl)-6-fluoro-1,2-benzisoxazole, 5.0 ml of pyrrolidine, 8.0 g of sodium bicarbonate, and a crystal of potassium iodide. After stirring at 70° C. for four hrs, the mixture was filtered and the filtrate was evaporated to an oil. The oil was stirred with 100 ml of water for five mins and then extracted with ether. The ether extract was washed with water (2x), saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After filtering, the solvent was evaporated to an oil. The oil was treated with ethereal oxalic acid, and the resultant salt was recrystallized twice from ethyl acetate/methanol/ether to give 2.7 g, (44%) of product, mp 190°-200° C. (dec).

Workup

  1. filtrationthe mixture was filtered
  2. customthe filtrate was evaporated to an oil
  3. stirringThe oil was stirred with 100 ml of water for five mins
  4. extractionextracted with ether
  5. extractionThe ether extract
  6. washwas washed with water (2x), saturated sodium chloride solution
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationAfter filtering
  9. customthe solvent was evaporated to an oil
  10. additionThe oil was treated with ethereal oxalic acid
  11. customthe resultant salt was recrystallized twice from ethyl acetate/methanol/ether

Sources & evidence

ORD record
ord-07bd7ae8ef6c44f794db0ef7f016ef66
Source dataset
uspto-grants-1986_05
Patent number
US04591586

Reaction notes

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