Triethylamine → HCID 86743145, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]([C:12](=[O:21])[C:13]1[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][C:14]=1[Cl:20])[CH2:7][CH2:6][C:5]2=[N:22][OH:23].C(N(CC)CC)C.[CH3:31][S:32](Cl)(=[O:34])=[O:33]>ClCCl>[S:32]([OH:34])(=[O:21])(=[O:33])[CH3:31].[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]([C:12](=[O:21])[C:13]1[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][C:14]=1[Cl:20])[CH2:7][CH2:6][C:5]2=[N:22][OH:23]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a mixture of 6-chloro-1-(2,4-dichlorobenzoyl)-2,3-dihydro-4(1H)-quinolinone-4-oxime (10.0 g), triethylamine (4.1 g) and dichloromethane (150 ml) was added dropwise methanesulfonyl chloride (3.5 g) at -20° C. with stirring. The mixture was stirred at -20° C. for 30 minutes and dichloromethane (300 ml) was added. The reaction mixture was sequentially washed with 1N HCl, saturated aqueous sodium bicarbonate solution, then with saturated aqueous NaCl solution and dried over anhydrous sodium sulfate. Solvent was removed in vacuo and the residue was recrystallized with ether and n-hexane to obtain 6-chloro-1-(2,4-dichlorobenzoyl)-2,3-dihydro-4(1H)-quinolinone-4-oxime mesylate (yield 11 g) as white crystal.
Workup
- stirringThe mixture was stirred at -20° C. for 30 minutes
- washThe reaction mixture was sequentially washed with 1N HCl, saturated aqueous sodium bicarbonate solution
- dry with materialwith saturated aqueous NaCl solution and dried over anhydrous sodium sulfate
- customSolvent was removed in vacuo
- customthe residue was recrystallized with ether and n-hexane
Sources & evidence
- ORD record
- ord-d029d351b3904685af155a7b98f7f411
- Source dataset
- uspto-grants-1989_06
- Patent number
- US04839368
Reaction notes
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