3-Chloro-4-(2-diethylaminoethoxy)phenylamine → HCID 10028442, compound

HRID 898580Notes

Reaction equation

HRID 898580 reaction equation
[Cl:1][C:2]1[CH:12]=[C:11]([C:13]2[CH:14]=[N:15][CH:16]=[CH:17][CH:18]=2)[CH:10]=[CH:9][C:3]=1[O:4][CH2:5][C:6]([OH:8])=O.[Cl:19][C:20]1[CH:21]=[C:22]([NH2:34])[CH:23]=[CH:24][C:25]=1[O:26][CH2:27][CH2:28][N:29]([CH2:32][CH3:33])[CH2:30][CH3:31]>>[Cl:19][C:20]1[CH:21]=[C:22]([NH:34][C:6](=[O:8])[CH2:5][O:4][C:3]2[CH:9]=[CH:10][C:11]([C:13]3[CH:14]=[N:15][CH:16]=[CH:17][CH:18]=3)=[CH:12][C:2]=2[Cl:1])[CH:23]=[CH:24][C:25]=1[O:26][CH2:27][CH2:28][N:29]([CH2:32][CH3:33])[CH2:30][CH3:31]

Participants

3

Reactant 2

HCID 167916763-Chloro-4-(2-diethylaminoethoxy)phenylamineHCID 68875873HCID 68875873, compound

Product 1

HCID 10028442HCID 10028442, compound

Procedure

The product was prepared according to general working method I from (2-chloro-4-pyridin-3-yl-phenoxy)-acetic acid (136b) and 3-chloro-4-(2-diethylamino-ethoxy)-phenylamine (Z1b).

Workup

  1. customThe product was prepared

Sources & evidence

ORD record
ord-bea3b4252e7843d9ba6d64c6ee31d7be
Source dataset
uspto-grants-2008_04
Patent number
US07351719B2

Reaction notes

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