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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430822Generated: November 1, 2026

Tetrabutylammonium Fluoride → HCID 86708501, compound

https://huagongshe.com/reaction/1430822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 86708500HCID 86708500—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86708501HCID 8670850196.7%

Reaction Steps

TBAF (1M in THF, 0.048 mL, 0.048 mmol) was added to a solution of N-((3R,4R)-1-(2-chloro-5-cyano-3-((7-cyano-4-(cyclopropylamino)imidazo[2,1-f][1,2,4]triazin-2-yl)amino)phenyl)-3-((triisopropylsilyl)oxy)piperidin-4-yl)methanesulfonamide (28 mg, 0.040 mmol) in THF (2 mL) and the reaction mixture was stirred at room temperature overnight. Solvent was evaporated and the crude product was purified by flash chromatography on silica gel using an automated ISCO system (12 g column, eluting with 0-6% methanol/dichloromethane). N-((3R,4R)-1-(2-chloro-5-cyano-3-((7-cyano-4-(cyclopropylamino)imidazo[2,1-f][1,2,4]triazin-2-yl)amino)phenyl)-3-hydroxypiperidin-4-yl)methanesulfonamide (21 mg) was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940736B2
Source datasetuspto-grants-2015_01
ORD IDord-25a7cc8e2ff64d28aba5893d9f2eb788
Source noteuspto-grants-2015_01