Piperidine → HCID 71217382, compound

HRID 1887959Notes

Reaction equation

HRID 1887959 reaction equation
[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6](=[O:32])[C:7]([CH2:18][NH:19][C:20](=[O:31])OC3C=CC([N+]([O-])=O)=CC=3)=[CH:8][N:9]2[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:4][CH:3]=1.[NH:33]1[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]1>>[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6](=[O:32])[C:7]([CH2:18][NH:19][C:20]([N:33]3[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]3)=[O:31])=[CH:8][N:9]2[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 8082PiperidineHCID 866757694-Nitrophenyl (7-chloro-4-oxo-1-phenyl-1,4-dihydroquinolin-3-yl)methylcarbamate

Product 1

HCID 71217382HCID 71217382, compound

Procedure

Piperidine-1-carboxylic acid (7-chloro-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-amide was prepared starting from intermediate M and piperidine. MS calcd. for C22H23ClN3O2 [(M+H)+] 396.1, obsd. 395.9.

Sources & evidence

ORD record
ord-a6f6a79607b34fe8b161395a9b4e3c84
Source dataset
uspto-grants-2013_08
Patent number
US08501732B2

Reaction notes

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