Hydrochloric Acid → (S)-N,N-DiMethyl-2-pyrrolidinecarboxaMide HCl
Reaction equation
C(OC([N:8]1[CH2:17][CH2:16][CH2:15][C@H:9]1[C:10]([N:12]([CH3:14])[CH3:13])=[O:11])=O)(C)(C)C.[ClH:18]>>[ClH:18].[CH3:13][N:12]([CH3:14])[C:10](=[O:11])[C@@H:9]1[CH2:15][CH2:16][CH2:17][NH:8]1Participants
3
Procedure
To the subtitle product of step i) (5.0 g) was added hydrochloric acid (20 ml, 4M). The mixture was stirred at room temperature for 3 h before the solvent was evaporated to afford the subtitle compound as a colourless solid. Yield: 3.50 g
Workup
- customwas evaporated
Sources & evidence
- ORD record
- ord-c6ab725a1dc04a6187594ecd46a41378
- Source dataset
- uspto-grants-2012_01
- Patent number
- US08106063B2
Reaction notes
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