4-(Piperidin-1-ylmethyl)aniline → HCID 59691704, compound

HRID 898582Notes

Reaction equation

HRID 898582 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([O:14][CH2:15][C:16]([OH:18])=O)=[CH:10][CH:9]=2)=[CH:4][CH:3]=1.[N:19]1([CH2:25][C:26]2[CH:31]=[CH:30][C:29]([NH2:32])=[CH:28][CH:27]=2)[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:9]=[CH:10][C:11]([O:14][CH2:15][C:16]([NH:32][C:29]3[CH:28]=[CH:27][C:26]([CH2:25][N:19]4[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]4)=[CH:31][CH:30]=3)=[O:18])=[CH:12][CH:13]=2)=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 8461504-(Piperidin-1-ylmethyl)anilineHCID 23036785HCID 23036785, compound

Product 1

HCID 59691704HCID 59691704, compound

Procedure

The product was prepared according to general working method I from (4′-chloro-biphenyl4-yloxy)-acetic acid (137a) and 4-piperidin-ylmethyl-phenylamine.

Workup

  1. customThe product was prepared

Sources & evidence

ORD record
ord-dd28cd0962604dfaa0e43d639cd6efa5
Source dataset
uspto-grants-2008_04
Patent number
US07351719B2

Reaction notes

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