1-Tert-butyl 4-chloromethyl piperidine-1,4-dicarboxylate → 4-Piperidinecarboxylic acid
Reaction equation
ClC1C=C(C=CC=1NC(=O)CC1CCCC1)C(NC1SC=CN=1)=O.ClC[O:27][C:28]([CH:30]1[CH2:35][CH2:34][N:33](C(OC(C)(C)C)=O)[CH2:32][CH2:31]1)=[O:29]>>[NH:33]1[CH2:34][CH2:35][CH:30]([C:28]([OH:29])=[O:27])[CH2:31][CH2:32]1Participants
3
Procedure
Prepared from 3-chloro-4-(2-cyclopentyl-acetylamino)-N-thiazol-2-yl-benzamide and piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-chloromethyl ester followed by deprotection.
Sources & evidence
- ORD record
- ord-f31094c4d411494a8d7c5aa52e5fa3cd
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07674912B2
Reaction notes
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