4-Piperidinecarboxamide → HCID 20253661, compound

HRID 638283Notes

Reaction equation

HRID 638283 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:17]=[C:16](Cl)[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[N:9]=2)=[CH:4][CH:3]=1.[NH:19]1[CH2:27][CH2:26][CH:22]([C:23]([NH2:25])=[O:24])[CH2:21][CH2:20]1>C(O)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:17]=[C:16]([N:19]3[CH2:27][CH2:26][CH:22]([C:23]([NH2:25])=[O:24])[CH2:21][CH2:20]3)[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[N:9]=2)=[CH:4][CH:3]=1

Participants

4

Reactant 2

HCID 37724-PiperidinecarboxamideHCID 136038992-(4-Bromophenyl)-4-chloroquinoline

Product 1

HCID 20253661HCID 20253661, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

The named compound was made in a manner analogous to that of Example 8(d) using (2-(4-bromophenyl)-4-chloroquinoline and isonipecotamide as starting materials. It was obtained as white needles, mp 247°-249° dec on recrystallization from ethanol.

Sources & evidence

ORD record
ord-cd8a9a37edb84ab7b4470fccba23231e
Source dataset
uspto-grants-1985_12
Patent number
US04560692

Reaction notes

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