Pyrrolidine → HCID 9859818, compound
Reaction equation
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH2:6]([C:8]1[C:12](=[O:13])[O:11][N:10]([C:14](Cl)=[O:15])[C:9]=1[CH2:17][CH2:18][CH3:19])[CH3:7]>ClCCl>[CH2:6]([C:8]1[C:12](=[O:13])[O:11][N:10]([C:14]([N:1]2[CH2:5][CH2:4][CH2:3][CH2:2]2)=[O:15])[C:9]=1[CH2:17][CH2:18][CH3:19])[CH3:7]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
At 0°C., a solution of 0.43 g (6 mmol) of pyrrolidine in 35 ml of dichloromethane are added dropwise to a solution of 0.44 g (2 mmol) of 4-ethyl-3-propyl-2-(chlorocarbonyl)-5(2H)-isoxazolone in 10 ml of dichloromethane, and the mixture is stirred at room temperature overnight. For work-up, the residue were chromatographed over silica gel using petroleum ether:ethyl acetate (4:1). MS (DCI): 253 (M+H).
Workup
- customFor work-up, the residue were chromatographed over silica gel
Sources & evidence
- ORD record
- ord-e2eab0930652498c98f78cbbe7026fd4
- Source dataset
- uspto-grants-2002_02
- Patent number
- US06344471B1
Reaction notes
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