Cyclopentanone → HCID 69592702, compound
Reaction equation
[C:1]([CH:8]([NH2:15])[CH:9]1[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].[C:16]1(=O)[CH2:20][CH2:19][CH2:18][CH2:17]1>>[C:1]([CH:8]([NH2:15])[CH:9]1[CH2:10][CH2:11][N:12]([CH:16]2[CH2:20][CH2:19][CH2:18][CH2:17]2)[CH2:13][CH2:14]1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2]Participants
3
Procedure
Using Alkylation Method B, 4-(Boc-aminomethyl)piperidine (15 g, 70 mmol) and cyclopentanone (36 g, 450 mmol) afforded 15.3 g (77%) of the title compound.
Sources & evidence
- ORD record
- ord-e975177fdb5d47bb90e66b875dc5615c
- Source dataset
- uspto-grants-2006_05
- Patent number
- US07053078B2
Reaction notes
Loading…