HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429680Generated: October 29, 2026
Trifluoroacetic acid → HCID 70139538, compound
https://huagongshe.com/reaction/429680
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 70120934 | HCID 70120934 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70139538 | HCID 70139538 | 87.1% |
Reaction Steps
To a solution of 4-[N-[1-[(tert-butyl)oxycarbonyl]benzimidazol-4-yl]carbamoyl]-N-[2-[4,4-dimethyl(2,5-oxazolinyl)]phenyl]-3-methoxy-N-methylbenzamide (400 mg) in dichloromethane (10 ml) was added trifluoroacetic acid (4 ml). The mixture was stirred at ambient temperature for 3 hours. The reaction mixture was concentrated in vacuo and the residue was diluted with a mixture of chloroform and saturated aqueous sodium bicarbonate solution. The organic layer was separated and washed with water and brine. The solution was dried over magnesium sulfate and the solvent was evaporated in vacuo. The residue was purified by column chromatography (chloroform:methanol=100:3) to give 4-[N-(1H-benzimidazol-4-yl)carbamoyl]-N-[2-[4,4-dimethyl(2,5-oxazolinyl)]phenyl]-3-methoxy-N-methylbenzamide (290 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06316482B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-dacd566713ee4ae4b0dee3ed0995e0d0 |
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| Source note | uspto-grants-2001_11 |
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