2,6-Dimethyl-1-piperidylamine → HCID 19376030, compound

HRID 2211189Notes

Reaction equation

HRID 2211189 reaction equation
[NH2:1][N:2]1[CH:7]([CH3:8])[CH2:6][CH2:5][CH2:4][CH:3]1[CH3:9].[Cl:10][C:11]1[CH:16]=[CH:15][C:14]([C:17]2[N:21]([C:22]3[CH:27]=[CH:26][C:25]([Cl:28])=[CH:24][C:23]=3[Cl:29])[N:20]=[C:19]([C:30](Cl)=[O:31])[CH:18]=2)=[CH:13][CH:12]=1>>[ClH:10].[CH3:9][CH:3]1[CH2:4][CH2:5][CH2:6][CH:7]([CH3:8])[N:2]1[NH:1][C:30]([C:19]1[CH:18]=[C:17]([C:14]2[CH:13]=[CH:12][C:11]([Cl:10])=[CH:16][CH:15]=2)[N:21]([C:22]2[CH:27]=[CH:26][C:25]([Cl:28])=[CH:24][C:23]=2[Cl:29])[N:20]=1)=[O:31]

Participants

3

Reactant 2

HCID 1234822,6-Dimethyl-1-piperidylamineHCID 54252626HCID 54252626, compound

Product 1

HCID 19376030HCID 19376030, compound

Procedure

This compound is prepared by the procedure described in EXAMPLE 1 starting from 1-amino-2,6-dimethylpiperidine and 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)pyrazole-3-carboxylic acid chloride. M.p.=195° C.

Workup

  1. customThis compound is prepared by the procedure

Sources & evidence

ORD record
ord-3299ed190a5546389456218425d3f289
Source dataset
uspto-grants-1995_10
Patent number
US05462960

Reaction notes

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