5-Methyl-2-pyrrolidone → HCID 71252478, compound
Reaction equation
I[C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8]CC)=[O:7])=[CH:4][CH:3]=1.[CH3:13][CH:14]1[NH:18][C:17](=[O:19])[CH2:16][CH2:15]1>>[CH3:13][CH:14]1[CH2:15][CH2:16][C:17](=[O:19])[N:18]1[C:2]1[CH:3]=[CH:4][C:5]([C:6]([OH:8])=[O:7])=[CH:11][CH:12]=1Participants
3
Procedure
Using ethyl 4-iodobenzoate (1.70 mL) and 5-methylpyrrolidin-2-one (0.98 g) and by the reaction and treatment in the same manner as in Preparation Example 15, the title compound (1.80 g) was obtained.
Workup
- customby the reaction and treatment in the same manner
- customas in Preparation Example 15
Sources & evidence
- ORD record
- ord-627a075a16ab449c86342e59236f5d1f
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08816079B2
Reaction notes
Loading…