Acetic Acid → 1-(3-Difluoromethyl-4-fluoro-phenyl)-1H-imidazole-4-carboxylic Acid

HRID 397925Notes

Reaction equation

HRID 397925 reaction equation
[F:1][CH:2]([F:11])[C:3]1[CH:4]=[C:5]([CH:7]=[CH:8][C:9]=1[F:10])[NH2:6].[CH:12](OCC)(OCC)OCC.[N+:22]([CH2:25]C(OCC)=O)([O-])=O.[C:31]([OH:34])(=[O:33])[CH3:32]>[Fe]>[F:11][CH:2]([F:1])[C:3]1[CH:4]=[C:5]([N:6]2[CH:12]=[C:32]([C:31]([OH:34])=[O:33])[N:22]=[CH:25]2)[CH:7]=[CH:8][C:9]=1[F:10]

Participants

6

Reactant 4

HCID 176Acetic Acid2×HCID 31214Ethyl orthoformate2×HCID 69379Ethyl nitroacetateHCID 234450763-(Difluoromethyl)-4-fluoroaniline

Product 1

HCID 234451291-(3-Difluoromethyl-4-fluoro-phenyl)-1H-imidazole-4-carboxylic Acid

Reagents, catalysts & solvents 1

HCID 23925IronCatalyst

Procedure

Following the general method described in example 234, 3-difluoromethyl-4-fluoroaniline was reacted with triethyl orthoformate, ethyl nitroacetate and acetic acid followed by treatment with triethyl orthoformate, iron and acetic acid and subsequent alkaline hydrolysis. The title compound was obtained as a light brown crystalline solid. Mp.>247° C. dec. (H2O/dioxane), MS: m/e=255 (M−H−).

Sources & evidence

ORD record
ord-c7027868dbfb4853b39202a738494c66
Source dataset
uspto-grants-2003_08
Patent number
US06610723B2

Reaction notes

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