Reaction equation
[Cl:1][C:2]1[N:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH3:12]N(C=O)C.C(Cl)(=O)C(Cl)=O>ClCCl>[Cl:1][C:2]1[N:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:3]=1[C:4]([O:6][CH3:12])=[O:5]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of 2-chloro-6-methylnicotinic acid (5.3 g, 30.8 mmol) in dichloromethane (100 ml) at 0° C. were added DMF (1 ml) and oxalyl chloride (3.2 ml, 36.9 mmol). The mixture was allowed to warmn to room temperature and stirred for 5 h. The solvents were removed in vacuo and the residue was dissolved in dichloromethane (50 ml) and methanol (50 ml). The mixture was stirred at room temperature for 18 h and then concentrated in vacuo. The residue was dissolved in chloroform, washed with saturated sodium bicarbonate solution and brine, dried over MgSO4, and concentrated in vacuo to give a brown oil; yield 5.70 g (100%).
Workup
- customto warmn to room temperature
- customThe solvents were removed in vacuo
- dissolutionthe residue was dissolved in dichloromethane (50 ml)
- stirringThe mixture was stirred at room temperature for 18 h
- concentrationconcentrated in vacuo
- dissolutionThe residue was dissolved in chloroform
- washwashed with saturated sodium bicarbonate solution and brine
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
- customto give a brown oil
Sources & evidence
- ORD record
- ord-e8a38c9878e446839eb2daf1c59b6e4a
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07176195B2
Linked notes
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