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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396178Generated: October 30, 2026

Trifluoroacetic acid → HCID 58485832, compound

https://huagongshe.com/reaction/1396178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 58485787HCID 58485787—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 58485832HCID 5848583281.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To [5-(7-benzenesulfonyl-4-cyclopropyl-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-6-fluoro-pyridin-2-yl]-(6-methoxy-pyridin-3-yl)-carbamic acid tert-butyl ester (77, 0.340 g, 0.527 mmol) in 10 mL of 1,2-dichloroethane, trifluoroacetic acid (0.80 mL, 10.4 mmol) is added. The reaction is stirred at 80° C. for 45 minutes, then poured into aqueous potassium carbonate and extracted with ethyl acetate. The organic layer is dried over sodium sulfate, filtered and the filtrate concentrated under vacuum to provide the desired compound (78, 235 mg). MS (ESI) [M+H+]+=545.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901118B2
Source datasetuspto-grants-2014_12
ORD IDord-748d870268a84899b3280ad8fbf74287
Source noteuspto-grants-2014_12