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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047137Generated: November 1, 2026

Trifluoroacetic anhydride → HCID 66735500, compound

https://huagongshe.com/reaction/2047137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantIodobenzeneHCID 11575—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantHCID 67494585HCID 67494585—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 66735500HCID 6673550019.5%

Reaction Steps

A solution of oxone (1.9 g, 3.1 mmol), trifluoroacetic anhydride (1.1 ml, 7.9 mmol) and H2O (5.7 ml) was stirred at 40° C. for 7 h, and then cooled to room temperature. To this a solution of tert-butyl 4-(6-acetyl-7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)-3-(6-phenylpyridin-3-yl)pyrazolo[1,5-a]pyrimidin-5-yl)piperidine-1-carboxylate (0.87 g, 1.13 mmol) and PhI (0.03 ml, 0.23 mmol) in acetonitrile (17 ml) was added. The resulting solution was stirred at 90° C. for 15 h. On cooling, the reaction mixture was filtered and solids were washed with DCM. It was then concentrated in vacuo to give a crude product which was submitted to the analytical group for purification to afford the desired 1-(7-amino-3-(6-phenylpyridin-3-yl)-5-(piperidin-4-yl)pyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyethanone (94.2 mg, 17%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08591943B2
Source datasetuspto-grants-2013_11
ORD IDord-d12c14484b0a4b59aa57732f47ac91d7
Source noteuspto-grants-2013_11