Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396175Generated: November 1, 2026

Trifluoroacetic acid → HCID 58485691, compound

https://huagongshe.com/reaction/1396175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 58485824HCID 58485824—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 58485691HCID 5848569171.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To {5-[(7-benzenesulfonyl-4-cyclopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-hydroxy-methyl]-6-fluoro-pyridin-2-yl}-(6-methoxy-pyridin-3-yl)-carbamic acid tert-butyl ester (75, 0.290 g, 0.448 mmol) in 9.93 mL of 1,2-dichloroethane, triethylsilane (0.31 mL, 2.0 mmol) and trifluoroacetic acid (0.16 mL, 2.0 mmol) are added and the reaction stirred at 80° C. for 4 hours. The reaction is poured into aqueous potassium carbonate and extracted with ethyl acetate. The organic layer is dried with sodium sulfate, filtered and the filtrate concentrated under vacuum to provide the desired compound (76, 170 mg). MS (ESI) [M+H+]+=530.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901118B2
Source datasetuspto-grants-2014_12
ORD IDord-376c90894018495aa359fe34337cd2a8
Source noteuspto-grants-2014_12