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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289236Generated: October 31, 2026

Trifluoroacetic acid → HCID 135848306, compound

https://huagongshe.com/reaction/1289236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPentafluorophenolHCID 13041—
ReactantPentafluorophenyl TrifluoroacetateHCID 4327891—
ReactantHCID 135966603HCID 135966603—
SolventPyridineHCID 1049—
SolventDimethylacetamideHCID 31374—
ProductHCID 135848306HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05747499
Source datasetuspto-grants-1998_05
ORD IDord-095be6ce2cdf4b5fb8a493ddb8ef0016
Source noteuspto-grants-1998_05