2,5-Dichlorobenzeneacetic acid → N-{[4-(3,4-Dichlorobenzyl)morpholin-2-yl]methyl}2-(2,5-dichlorophenyl)acetamide

HRID 2211992Notes

Reaction equation

HRID 2211992 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:14]=[CH:15][C:16]=1[Cl:17])[CH2:5][N:6]1[CH2:11][CH2:10][O:9][CH:8]([CH2:12][NH2:13])[CH2:7]1.[Cl:18][C:19]1[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][C:20]=1[CH2:26][C:27](O)=[O:28]>>[Cl:1][C:2]1[CH:3]=[C:4]([CH:14]=[CH:15][C:16]=1[Cl:17])[CH2:5][N:6]1[CH2:11][CH2:10][O:9][CH:8]([CH2:12][NH:13][C:27](=[O:28])[CH2:26][C:20]2[CH:21]=[C:22]([Cl:25])[CH:23]=[CH:24][C:19]=2[Cl:18])[CH2:7]1

Participants

3

Reactant 2

HCID 947882,5-Dichlorobenzeneacetic acidHCID 10308229[4-(3,4-Dichlorobenzyl)morpholin-2-yl]methylamine

Product 1

HCID 21962845N-{[4-(3,4-Dichlorobenzyl)morpholin-2-yl]methyl}2-(2,5-dichlorophenyl)acetamideYield 27.1%

Procedure

Example 13 was prepared in an analogous manner to Example 4 using a mixture of Intermediate 1 (0.055 g) and (2,5-dichlorophenyl)acetic acid (0.041 g) to give the title compound (0.025 g).

Workup

  1. customExample 13 was prepared in an analogous manner to Example 4 using

Sources & evidence

ORD record
ord-4753cd2ed81e44c9a51163429cc6536c
Source dataset
uspto-grants-2006_09
Patent number
US07101882B2

Reaction notes

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