HCID 15165792, compound → HCID 15165793, compound
Reaction equation
[N:1]1([C:6]([CH:8]2[CH2:13][CH2:12][C:11]([CH3:15])([CH3:14])[CH2:10][NH:9]2)=O)[CH2:5][CH2:4][CH2:3][CH2:2]1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[N:1]1([CH2:6][CH:8]2[CH2:13][CH2:12][C:11]([CH3:15])([CH3:14])[CH2:10][NH:9]2)[CH2:2][CH2:3][CH2:4][CH2:5]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
By reducing 3.3 g (15.69 mmoles) of 2-(pyrrolidin-1-yl)carbonyl-5,5-dimethyl piperidine with 0.89 g (23.5 mmoles) of LiAlH4 in 80 ml of dry THF, using an alkaline work-up, 2.5 g of the title compound were obtained. The compound was sufficiently pure for the following step.
Sources & evidence
- ORD record
- ord-11730d73d6444341beeb452fd60ef55b
- Source dataset
- uspto-grants-1992_02
- Patent number
- US05089507
Reaction notes
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