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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385682Generated: October 28, 2026

2-(Tri-n-butylstannyl)oxazole → HCID 57815469, compound

https://huagongshe.com/reaction/385682

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tri-n-butylstannyl)oxazoleHCID 15486183—
ReactantHCID 57815264HCID 57815264—
CatalystHCID 178418851HCID 178418851—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57815469HCID 5781546988.8%

Reaction Steps

To a solution of 0.10 g of tert-butyl (1-(2-(7-bromo-2-oxo-1,5-naphthyridin-1(2H)-yl)ethyl)piperidin-4-yl)(2,3-dihydro(1,4)dioxino(2,3-c)pyridin-7-ylmethyl)carbamate in 2 mL of dioxane, 90 mg of 2-tributylstannyloxazole and 17 mg of bis(tri-tert-butylphosphine)palladium(0) were added under a nitrogen atmosphere, and the mixture was heated under reflux while stirring for 6 hours 30 minutes. The resultant residue was purified by flash silica gel column chromatography using gradient elution with chloroform:methanol=98:2 to 95:5 to obtain 87 mg of tert-butyl (2,3-dihydro(1,4)dioxino(2,3-c)pyridin-7-ylmethyl)(1-(2-(7-(1,3-oxazol-2-yl)-2-oxo-1,5-naphthyridin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367831B2
Source datasetuspto-grants-2013_02
ORD IDord-5511bb0977de46efab9a811e8914f0de
Source noteuspto-grants-2013_02