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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259185Generated: November 2, 2026

Tetrabutylammonium Fluoride → HCID 58213470, compound

https://huagongshe.com/reaction/1259185

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 numberUS08466167B2
Source datasetuspto-grants-2013_06
ORD IDord-88cc52703e0b4c3885e3ae9672632421
Source noteuspto-grants-2013_06