Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047388Generated: November 1, 2026

N-(2-amino-phenyl)-5-bromo-2-fluoro-benzamide → 2-(5-Bromo-2-fluoro-phenyl)-1H-benzoimidazole

https://huagongshe.com/reaction/2047388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-amino-phenyl)-5-bromo-2-fluoro-benzamideHCID 24693313—
SolventAcetic AcidHCID 176—
Product2-(5-Bromo-2-fluoro-phenyl)-1H-benzoimidazoleHCID 4323645189.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

A suspension of N-(2-amino-phenyl)-5-bromo-2-fluoro-benzamide (5.64 g, 18.3 mmol) in acetic acid (20 mL) was heated at 60° C. After 30 min, the suspension became a solution and it was left overnight. The solvent was removed under reduced pressure and residue was triturated with DCM (10 mL) and filtered off. The precipitate was washed with DCM (3×10 mL) and dried to afford 4.76 g of the title compound (89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592463B2
Source datasetuspto-grants-2013_11
ORD IDord-a0020226a2894bd2a1ecc68c4a8d1139
Source noteuspto-grants-2013_11