HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289236Generated: October 31, 2026
Trifluoroacetic acid → HCID 135848306, compound
https://huagongshe.com/reaction/1289236
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Pentafluorophenol | HCID 13041 | — |
| Reactant | Pentafluorophenyl Trifluoroacetate | HCID 4327891 | — |
| Reactant | HCID 135966603 | HCID 135966603 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 135848306 | HCID 135848306 | — |
Reaction Steps
A mixture of 5-[N-methyl-N-((6RS)-2-methyl-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)amino]pyridine-2-carboxylic acid (0.01 g), pentafluorophenyl trifluoroacetate (0.16 g; prepared by the reaction of pentafluorophenol and trifluoroacetic acid), pyridine (0.045 g) and DMA (5 ml) was stirred at ambient temperature for 5 hours. The mixture was evaporated and the residue was partitioned between ethyl acetate and a saturated aqueous sodium bicarbonate solution. The organic phase was dried (MgSO4) and evaporated. The residue was purified by column chromatography using increasingly polar mixtures of ethyl acetate and methanol as eluant. There was thus obtained pentafluorophenyl 5-[N-methyl-N-((6RS)-2-methyl-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)amino]-pyridine-2-carboxylate as a foam (0.1 g);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05747499 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-095be6ce2cdf4b5fb8a493ddb8ef0016 |
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| Source note | uspto-grants-1998_05 |
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