Piperidine → 1-[3-(4-Pyridinylamino)benzoyl]piperidine

HRID 64897Notes

Reaction equation

HRID 64897 reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([NH:7][C:8]2[CH:9]=[C:10]([CH:14]=[CH:15][CH:16]=2)[C:11]([OH:13])=O)=[CH:3][CH:2]=1.[NH:17]1[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]1>>[N:1]1[CH:2]=[CH:3][C:4]([NH:7][C:8]2[CH:9]=[C:10]([CH:14]=[CH:15][CH:16]=2)[C:11]([N:17]2[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]2)=[O:13])=[CH:5][CH:6]=1

Participants

3

Reactant 2

HCID 8082PiperidineHCID 137124753-[(Pyridin-4-yl)amino]benzoic acid

Product 1

HCID 137124771-[3-(4-Pyridinylamino)benzoyl]piperidine

Procedure

1-[3-(4-Pyridinylamino)benzoyl]piperidine was prepared from 3-(4-pyridinylamino)benzoic acid and piperidine according to a procedure analogous to that of Example 48(b), and was obtained in the form of its hydrochloride salt, colorless powder, m.p. 224°-226° C. when recrystallized from ethanol.

Sources & evidence

ORD record
ord-bc4daf8d6580406caa1a427e8ba116e0
Source dataset
uspto-grants-1986_09
Patent number
US04610991

Reaction notes

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