5-(1-Benzyloxycarbonyl-4-piperidyl)pentanol → Phenylmethyl 4-(5-bromopentyl)-1-piperidinecarboxylate
Reaction equation
[Br:1]CCCC1CCCCN1C(OCC1C=CC=CC=1)=O.O[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH:27]1[CH2:32][CH2:31][N:30]([C:33]([O:35][CH2:36][C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)=[O:34])[CH2:29][CH2:28]1>>[Br:1][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH:27]1[CH2:32][CH2:31][N:30]([C:33]([O:35][CH2:36][C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)=[O:34])[CH2:29][CH2:28]1Participants
3
Procedure
Prepared similarly to Intermediate 30 from phenylmethyl 4-(5-hydroxypentyl)-1-piperidinecarboxylate.
Sources & evidence
- ORD record
- ord-b5deb1d3d78a40a38c7b9867063d2443
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08802684B2
Reaction notes
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