Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403781Generated: November 2, 2026

3-(1,3-Dioxolan-2-yl)-phenyl-tributylstannane → (4-Benzyloxy-phenyl)-(6-(3-(1,3-dioxolan-2-yl)-phenyl)-pyrido[3,4-d]pyrimidin-4-yl)-amine

https://huagongshe.com/reaction/1403781

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1,3-Dioxolan-2-yl)-phenyl-tributylstannaneHCID 15254934—
Reactant4-(4-Benzyloxyanilino)6-chloropyrido[3,4-d]pyrimidineHCID 21952168—
Solvent1,4-DioxaneHCID 31275—
Product(4-Benzyloxy-phenyl)-(6-(3-(1,3-dioxolan-2-yl)-phenyl)-pyrido[3,4-d]pyrimidin-4-yl)-amineHCID 2272513113.7%

Reaction Steps

(4-Benzyloxy-phenyl)-(6-chloro-pyrido[3,4-d]pyrimidin-4-yl)-amine (1.4 g) and 3-(1,3-dioxolan-2-yl)-phenyl-tributylstannane (3.08 g) [A. Lee and W-C. Dai, Tetrahedron (1997), 53(3), 859-868] in dioxan (30 ml) were reacted together as in Procedure B. The mixture was evaporated and the residue suspended in dichloromethane. This was then filtered through celite and the solvent evaporated. The gummy residue was then triturated with hexane giving a beige solid. This material was further purified by column chromatography, giving a brown foam (252 mg); m/z 477 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912205B2
Source datasetuspto-grants-2014_12
ORD IDord-e6e673d832814405858fd913737ac1a4
Source noteuspto-grants-2014_12