2-Methylbenzoyl chloride → HCID 15887624, compound

HRID 377114Notes

Reaction equation

HRID 377114 reaction equation
[Cl:1][C:2]1[CH:16]=[CH:15][C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([NH:13][CH3:14])=[CH:9][N:8]=2)=[C:4]([CH3:17])[CH:3]=1.[CH3:18][C:19]1[CH:27]=[CH:26][CH:25]=[CH:24][C:20]=1[C:21](Cl)=[O:22].ClC1C=CC=C(Cl)C=1C(N(C1C=NC(OC2C=CC(Cl)=CC=2C)=CC=1)C)=O>>[CH3:18][C:19]1[CH:27]=[CH:26][CH:25]=[CH:24][C:20]=1[C:21]([N:13]([C:10]1[CH:9]=[N:8][C:7]([O:6][C:5]2[CH:15]=[CH:16][C:2]([Cl:1])=[CH:3][C:4]=2[CH3:17])=[CH:12][CH:11]=1)[CH3:14])=[O:22]

Participants

4

Reactant 3

HCID 702762-Methylbenzoyl chlorideHCID 15887622HCID 15887622, compoundHCID 18419445HCID 18419445, compound

Product 1

HCID 15887624HCID 15887624, compound

Procedure

2-Methyl-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-methylbenzoyl 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-f2f03d6f4e6d4b9f95c247eee3af3f3e
Source dataset
uspto-grants-2000_02
Patent number
US06022884

Reaction notes

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