2-Bromo-4-chloro-6-fluoroaniline → N,N-dimethyl-5-ethyl-2-(2'-bromo-4'-chloro-6'-fluoroanilino)phenylacetamide

HRID 382495Notes

Reaction equation

HRID 382495 reaction equation
[CH3:1][N:2]([CH3:15])[C:3](=[O:14])[CH2:4][C:5]1[CH:10]=[C:9]([CH2:11][CH3:12])[CH:8]=[CH:7][C:6]=1I.[Br:16][C:17]1[CH:23]=[C:22]([Cl:24])[CH:21]=[C:20]([F:25])[C:18]=1[NH2:19]>>[CH3:1][N:2]([CH3:15])[C:3](=[O:14])[CH2:4][C:5]1[CH:10]=[C:9]([CH2:11][CH3:12])[CH:8]=[CH:7][C:6]=1[NH:19][C:18]1[C:20]([F:25])=[CH:21][C:22]([Cl:24])=[CH:23][C:17]=1[Br:16]

Participants

3

Reactant 2

HCID 27362222-Bromo-4-chloro-6-fluoroanilineHCID 21938643N,N-dimethyl-5-ethyl-2-iodophenylacetamide

Product 1

HCID 86584270N,N-dimethyl-5-ethyl-2-(2'-bromo-4'-chloro-6'-fluoroanilino)phenylacetamide

Procedure

Ullmann condensation of N,N-dimethyl-5-ethyl-2-iodo-phenylacetamide with 2-bromo-4-chloro-6-fluoroaniline according to the procedure described in Example 1 yields N,N-dimethyl-5-ethyl-2-(2′-bromo-4′-chloro-6′-fluoroanilino)phenylacetamide.

Sources & evidence

ORD record
ord-b6cd2e89b42a47bdbb6438e99248afce
Source dataset
uspto-grants-2001_10
Patent number
US06310099B1

Reaction notes

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