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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696723Generated: November 1, 2026

Trifluoroacetic anhydride → HCID 59004196, compound

https://huagongshe.com/reaction/1696723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 59004214HCID 59004214—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 59004196HCID 59004196—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of N5-(2-Amino-4-methoxy-phenyl)-pyridine-2,5-diamine (150 mg, 0.65 mmol) in trifluoroacetic acid (5 ml) was added (CF3CO)2O (5 ml). The resultant solution was allowed to stir at 80° C. for 4 hours. The reaction progress was monitored by TLC (EtOAc/petroleum ether=1:2). The mixture was concentrated under reduced pressure on a rotary evaporator. The reaction mixture was then quenched by adding 30 ml of 10% NaHCO3. The resultant solution was extracted three times with 50 ml of EtOAc and the organic layers were combined and dried over Na2SO4. After removal of the drying reagent by filtration, the crude product, 2,2,2-Trifluoro-N-[5-(5-methoxy-2-trifluoromethyl-benzoimidazol-1-yl)-pyridin-2-yl]-acetamide (ff), was obtained by removal of the solvent under reduced pressure and it was used directly in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163777B2
Source datasetuspto-grants-2012_04
ORD IDord-a58991fa590b49e1a4f32ac78ac38c68
Source noteuspto-grants-2012_04