Chloroform → HCID 14207290, compound

HRID 1085118Notes

Reaction equation

HRID 1085118 reaction equation
[C:1]1([N:7]2[CH:11]=[CH:10][N:9]=[C:8]2[S:12]([CH2:14][C:15]([C:17]2[CH:18]=[C:19]3[C:24](=[CH:25][CH:26]=2)[NH:23][C:22](=[O:27])[CH2:21][CH2:20]3)=[O:16])=[O:13])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Mn]([O-])(=O)(=O)=[O:29].[K+].C(Cl)(Cl)Cl>C(O)(=O)C.O>[C:1]1([N:7]2[CH:11]=[CH:10][N:9]=[C:8]2[S:12]([CH2:14][C:15]([C:17]2[CH:18]=[C:19]3[C:24](=[CH:25][CH:26]=2)[NH:23][C:22](=[O:27])[CH2:21][CH2:20]3)=[O:16])(=[O:29])=[O:13])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Participants

6

Procedure

3.79 Grams (10 mM) of 6-[2-(1-phenyl-2-imidazolyl)sulfinylacetyl]-3,4-dihydrocarbostyril was dissolved in a mixture of 240 ml of acetic acid with 100 ml of water, then 5.06 g (32 mM) of potassium permanganate was added thereto. This mixture was stirred at room temperature for 2 days. After the reaction was completed, chloroform was added to the reaction mixture and filtered with Celite (a trademark for distomaceous earth product, manufactured by Johns-Manville Products Corp.). The filtrate was washed with water and dried with anhydrous magnensium sulfate. The residue obtained by removing the solvent was purified by means of a silica gel column chromatography (eluent: chloroform : methanol=30:1), and recrystallized from ethanol-chloroform to yield 0.6 g of 6-[2-(1-phenyl-2-imidazolyl)sulfonylacetyl]-3,4-dihydrocarbostyril. Light yellow granular substance.

Workup

  1. filtrationfiltered with Celite (a trademark for distomaceous earth product
  2. washThe filtrate was washed with water
  3. dry with materialdried with anhydrous magnensium sulfate
  4. customThe residue obtained
  5. customby removing the solvent
  6. customwas purified by means of a silica gel column chromatography (eluent: chloroform : methanol=30:1)
  7. customrecrystallized from ethanol-chloroform

Sources & evidence

ORD record
ord-c20247f78a9b48f39198deada727ea9c
Source dataset
uspto-grants-1991_04
Patent number
US05008274

Reaction notes

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