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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192815Generated: November 2, 2026

Trifluoroacetic anhydride → HCID 86649290, compound

https://huagongshe.com/reaction/2192815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactanttert-butyl (3R*,5S*)-3-(aminocarbonyl)-5-[({2-tert-butyl-4-[(2-furylmethyl)amino]pyrimidin-5-yl}carbonyl)(isobutyl)amino]piperidine-1-carboxylateHCID 59625490—
SolventPyridineHCID 1049—
ProductHCID 86649290HCID 8664929088.6%

Reaction Steps

tert-Butyl (3R*,5S*)-3-(aminocarbonyl)-5-[({2-tert-butyl-4-[(2-furylmethyl)amino]pyrimidin-5-yl}carbonyl)(isobutyl)amino]piperidine-1-carboxylate (469 mg) was dissolved in pyridine (5 ml), trifluoroacetic anhydride (0.25 ml) was added under ice-cooling, and the mixture was stirred at room temperature for 11 hr. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with ethyl acetate. The solution was washed successively with 1 M hydrochloric acid and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography, and the fraction eluted with ethyl acetate-hexane (5:95-80:20) was concentrated under reduced pressure to give the object compound (402 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329691B2
Source datasetuspto-grants-2012_12
ORD IDord-39bc9bc889ea424c92a4873ba653291e
Source noteuspto-grants-2012_12