HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696723Generated: November 1, 2026
Trifluoroacetic anhydride → HCID 59004196, compound
https://huagongshe.com/reaction/1696723
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | HCID 59004214 | HCID 59004214 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 59004196 | HCID 59004196 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163777B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-a58991fa590b49e1a4f32ac78ac38c68 |
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| Source note | uspto-grants-2012_04 |
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