2,4-Dichlorobenzoic Acid → HCID 73672707, compound

HRID 1482566Notes

Reaction equation

HRID 1482566 reaction equation
[Cl:1][C:2]1[CH:10]=[C:9]([Cl:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.[Cl:12][CH:13]1[CH2:18][CH2:17][N:16]([CH:19]([C:22]2[CH:23]=[N:24][C:25]([CH3:28])=[N:26][CH:27]=2)[CH2:20][NH2:21])[CH2:15][CH2:14]1>>[Cl:1][C:2]1[CH:10]=[C:9]([Cl:11])[CH:8]=[CH:7][C:3]=1[C:4]([NH:21][CH2:20][CH:19]([N:16]1[CH2:15][CH2:14][CH:13]([Cl:12])[CH2:18][CH2:17]1)[C:22]1[CH:23]=[N:24][C:25]([CH3:28])=[N:26][CH:27]=1)=[O:6]

Participants

3

Reactant 2

HCID 57872,4-Dichlorobenzoic AcidHCID 86716048HCID 86716048, compound

Product 1

HCID 73672707HCID 73672707, compound

Procedure

From 2,4-dichlorobenzoic acid and 2-(4-chloropiperidin-1-yl)-2-(2-methylpyrimidin-5-yl)ethanamine.

Sources & evidence

ORD record
ord-58dd4d0c96574d67a104c4bf19d12804
Source dataset
uspto-grants-2016_08
Patent number
US09415055B2

Reaction notes

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