Pyrrolidine → t-Butyl 3-[4-(dimethylamino)-2-butynyl]-2-oxo-1-imidazolidinecarboxylate
Reaction equation
N1CC[CH2:3][CH2:2]1.[C:6]([O:10][C:11]([N:13]1[CH2:17][CH2:16][NH:15][C:14]1=[O:18])=[O:12])([CH3:9])([CH3:8])[CH3:7].[CH3:19][N:20]1[CH2:24][CH2:23]N[C:21]1=O>>[CH3:19][N:20]([CH3:21])[CH2:24][C:23]#[C:2][CH2:3][N:15]1[CH2:16][CH2:17][N:13]([C:11]([O:10][C:6]([CH3:9])([CH3:7])[CH3:8])=[O:12])[C:14]1=[O:18]Participants
4
Procedure
This product, a liquid, was prepared according to Example 1 by substituting dimethylamine for pyrrolidine and 1-t-butoxycarbonyl-2-imidazolidinone for 1-methyl-2-imidazolidinone.
Workup
- customThis product, a liquid, was prepared
Sources & evidence
- ORD record
- ord-95bba8aa1f154b7bb360250663be4682
- Source dataset
- uspto-grants-1992_10
- Patent number
- US05157124
Reaction notes
Loading…