Dimethyl Sulfoxide → HCID 59398262, compound

HRID 39731Notes

Reaction equation

HRID 39731 reaction equation
C(Cl)(Cl)Cl.C(Cl)(=O)C(Cl)=O.CS(C)=O.[OH:15][CH2:16][CH2:17][N:18]1[C:27]2[C:22](=[CH:23][CH:24]=[C:25]([Cl:28])[CH:26]=2)[C:21]([Cl:29])=[CH:20][C:19]1=[O:30]>O.C(N(CC)CC)C>[Cl:29][C:21]1[C:22]2[C:27](=[CH:26][C:25]([Cl:28])=[CH:24][CH:23]=2)[N:18]([CH2:17][CH:16]=[O:15])[C:19](=[O:30])[CH:20]=1

Participants

7

Procedure

To 2 mL of a chloroform solution containing 54 mg of oxalyl chloride, 64 mg of dimethyl sulfoxide was added dropwise at −60° C., and the mixture was stirred for 15 minutes. Thereto was added dropwise 2 mL of a chloroform solution containing 85 mg of 1-(2-hydroxyethyl)-4,7-dichloroquinolin-2(1H)-one at the same temperature, and the reaction mixture was stirred for 15 minutes. Thereto was added 133 mg of triethylamine at the same temperature, then the mixture was stirred at room temperature for 45 minutes, and water was added thereto. The organic layer was separated, washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [silica gel; Silica gel 60N manufactured by Kanto Chemical Co., Inc., eluent; chloroform:methanol=10:1] to obtain 69 mg of a brown oily substance, (4,7-dichloro-2-oxoquinolin-1(2H)-yl)acetaldehyde.

Workup

  1. additionwas added dropwise at −60° C.
  2. stirringthe reaction mixture was stirred for 15 minutes
  3. stirringthe mixture was stirred at room temperature for 45 minutes
  4. customThe organic layer was separated
  5. washwashed with an aqueous saturated sodium chloride solution
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customthe solvent was removed under reduced pressure
  8. customThe residue thus obtained
  9. customwas purified by silica gel column chromatography [silica gel; Silica gel 60N manufactured by Kanto Chemical Co., Inc., eluent; chloroform:methanol=10:1]

Sources & evidence

ORD record
ord-e32b8dc86a38450ca5d82be7f70ad02a
Source dataset
uspto-grants-2013_09
Patent number
US08524738B2

Reaction notes

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