4-Piperidinecarboxamide → HCID 13603930, compound

HRID 638298Notes

Reaction equation

HRID 638298 reaction equation
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([CH3:12])[CH:10]=2)[N:5]=[C:4]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:3]=1.[NH:19]1[CH2:27][CH2:26][CH:22]([C:23]([NH2:25])=[O:24])[CH2:21][CH2:20]1>N1C=CC=CC=1>[CH3:12][C:9]1[CH:10]=[C:11]2[C:6](=[CH:7][CH:8]=1)[N:5]=[C:4]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[CH:3]=[C:2]2[N:19]1[CH2:27][CH2:26][CH:22]([C:23]([NH2:25])=[O:24])[CH2:21][CH2:20]1

Participants

4

Reactant 2

HCID 37724-PiperidinecarboxamideHCID 70221594-Chloro-6-methyl-2-phenylquinoline

Product 1

HCID 13603930HCID 13603930, compound

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

The named compound was made in a manner analogous to that of Example 4(c) using 4-chloro-6-methyl-2-phenylquinoline and isonipecotamide as starting materials. It was obtained as white solid, mp 245°-247° dec on recrystallization from pyridine.

Sources & evidence

ORD record
ord-a7f6d61866c4454b872f1c3573148ed3
Source dataset
uspto-grants-1985_12
Patent number
US04560692

Reaction notes

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