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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035553Generated: November 2, 2026

Tetrabutylammonium Fluoride → HCID 136337804, compound

https://huagongshe.com/reaction/2035553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant2-([1,2,4]Triazolo[4,3-a]pyridin-3-yl)-8-(tert-butyldimethylsilyloxy) quinolineHCID 67231442—
SolventTetrahydrofuranHCID 8028—
ProductHCID 136337804HCID 13633780490.4%

Reaction Steps

To a solution of 2-([1,2,4]triazolo[4,3-a]pyridin-3-yl)-8-(tert-butyldimethylsilyloxy) quinoline (18.92 g, 50.25 mmol) in anhydrous THF (400 mL) at 0° C. was added tetrabutylammonium fluoride (75.4 mL, 1.0 M/THF, 75.4 mmol). After stirring for 1 hour at this temperature the mixture was partitioned between saturated NaHCO3 and EtOAc. The aqueous phase was extracted with EtOAc and the combined organic phases were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was triturated with CH2Cl2, filtered and dried in vacuo to provide 11.91 g (90%) of desired product as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575145B2
Source datasetuspto-grants-2013_11
ORD IDord-72827fa4814249ac8503cc48274ea3ac
Source noteuspto-grants-2013_11