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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468895Generated: October 30, 2026

tert-Butyl(dimethyl)[(prop-2-yn-1-yl)oxy]silane → 3-((Tert-butyldimethylsilyloxy)methyl)-7-chloro-2,6-naphthyridine

https://huagongshe.com/reaction/468895

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl(dimethyl)[(prop-2-yn-1-yl)oxy]silaneHCID 3445622—
ReactantN-((5-bromo-2-chloropyridin-4-yl)methylene)-2-methylpropan-2-amineHCID 86674941—
CatalystZincHCID 23994—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product3-((Tert-butyldimethylsilyloxy)methyl)-7-chloro-2,6-naphthyridineHCID 86674968—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of N-((5-bromo-2-chloropyridin-4-yl)methylene)-2-methylpropan-2-amine (530 mg, 1.9 mmol), tert-butyldimethyl(2-propynyloxy)silane (0.59 mL, 2.9 mmol), NiCl2(DPPP) (52 mg, 0.1 mmol), and zinc (252 mg, 3.9 mmol) in acetonitrile (5 mL) was heated at 70° C. under an atmosphere of nitrogen. The cooled reaction mixture was diluted with methylene chloride (50 mL), filtered over Celite, and evaporated in vacuo to afford a residue that was purified by flash chromatography (silica, 12 g, ISCO, 0-40% ethyl acetate in heptane) to afford the title compound as an orange waxy solid (340 mg, 57%), which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623889B2
Source datasetuspto-grants-2014_01
ORD IDord-0213543d3db54f06a13f9349ede95e74
Source noteuspto-grants-2014_01