Ethyl 4-piperidinecarboxylate → HCID 58478839, compound
Reaction equation
[O:1]=[C:2]1[C:10]2[C:5](=[N:6][C:7]([CH2:11][CH2:12][CH:13]=O)=[CH:8][CH:9]=2)[CH2:4][O:3]1.[NH:15]1[CH2:25][CH2:24][CH:18]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[CH2:17][CH2:16]1>>[CH2:22]([O:21][C:19]([CH:18]1[CH2:24][CH2:25][N:15]([CH2:13][CH2:12][CH2:11][C:7]2[N:6]=[C:5]3[CH2:4][O:3][C:2](=[O:1])[C:10]3=[CH:9][CH:8]=2)[CH2:16][CH2:17]1)=[O:20])[CH3:23]Participants
3
Procedure
In a process similar to that described in Preparation 8 3-(5-oxo-5,7-dihydro-furo[3,4-b]pyridin-2-yl)-propionaldehyde (76 mg, 0.4 mmol) and ethyl isonipecotate (62 μL, 0.4 mmol) are reacted to provide the title compound as white solid (110 mg, 83%).
Workup
- customare reacted
Sources & evidence
- ORD record
- ord-7fa96fce843d467085601b5a18cfe0b2
- Source dataset
- uspto-grants-2013_06
- Patent number
- US08455535B2
Reaction notes
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