2-Chlorobenzoyl chloride → HCID 15887623, compound

HRID 377113Notes

Reaction equation

HRID 377113 reaction equation
ClC1C=CC(OC2C=CC(NC)=CN=2)=C(C)C=1.ClC1C=CC=CC=1C(Cl)=O.[Cl:28][C:29]1[CH:53]=[CH:52][CH:51]=[C:50](Cl)[C:30]=1[C:31]([N:33]([C:35]1[CH:36]=[N:37][C:38]([O:41][C:42]2[CH:47]=[CH:46][C:45]([Cl:48])=[CH:44][C:43]=2[CH3:49])=[CH:39][CH:40]=1)[CH3:34])=[O:32]>>[Cl:28][C:29]1[CH:53]=[CH:52][CH:51]=[CH:50][C:30]=1[C:31]([N:33]([C:35]1[CH:36]=[N:37][C:38]([O:41][C:42]2[CH:47]=[CH:46][C:45]([Cl:48])=[CH:44][C:43]=2[CH3:49])=[CH:39][CH:40]=1)[CH3:34])=[O:32]

Participants

4

Reactant 3

HCID 691102-Chlorobenzoyl chlorideHCID 15887622HCID 15887622, compoundHCID 18419445HCID 18419445, compound

Product 1

HCID 15887623HCID 15887623, compound

Procedure

2-Chloro-N-(6-(4-chloro-2-methyl-phenoxy)-pyridin-3-yl)-N-methyl-benzamide was prepared from 2-(4-Chloro-2-methyl-phenoxy)-5-(N-methylamino)pyridine and 2-chlorobenzoyl chloride in the same manner as 2,6-Dichloro-N-(6-(4-chloro-2-methyl-phenoxy)-pyridin-3-yl)-N-methyl-benzamide was prepared.

Workup

  1. customwas prepared

Sources & evidence

ORD record
ord-bd13d1cf8f054f3295080ed97a591c70
Source dataset
uspto-grants-2000_02
Patent number
US06022884

Reaction notes

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