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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479604Generated: October 30, 2026

Tetrabutylammonium Fluoride → HCID 58213470, compound

https://huagongshe.com/reaction/1479604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 86652357HCID 86652357—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58213470HCID 58213470—

Reaction Steps

A solution of 8-((tert-butyldimethylsilyloxy)methyl)-3-chlorobenzo[f][1,7]naphthyridin-5-amine (from the previous step) (1.0 eq.) and TBAF (1.1 eq.) in THF was stirred at ambient temperature overnight. The reaction was quenched with saturated NaHCO3. The two phases were separated, and the aqueous layer was extracted twice with Et2O. The combined organic layers were washed with brine, dried over anhydrous MgSO4, and concentrated en vaccuo. The crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-5% MeOH/DCM to give (5-amino-3-chlorobenzo[f][1,7]naphthyridin-8-yl)methanol as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09408907B2
Source datasetuspto-grants-2016_08
ORD IDord-4948cc763ccd4ede869396b1abb46b5f
Source noteuspto-grants-2016_08