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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51139Generated: October 26, 2026

Stannane, tributyl[5-(1,3-dioxolan-2-yl)-2-furanyl]- → (6-(5-(1,3-Dioxolan-2-yl)-furan-2-yl)-pyrido[3,4-d]pyrimidin-4-yl)-(4-(3-fluorobenzyloxy)-phenyl)-amine

https://huagongshe.com/reaction/51139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannane, tributyl[5-(1,3-dioxolan-2-yl)-2-furanyl]-HCID 10960952—
Reactant(6-Chloropyrido[3,4-d]pyrimidin-4-yl)-(4-(3-fluorobenzyloxy)-phenyl)-amineHCID 21952062—
Solvent1,4-DioxaneHCID 31275—
Product(6-(5-(1,3-Dioxolan-2-yl)-furan-2-yl)-pyrido[3,4-d]pyrimidin-4-yl)-(4-(3-fluorobenzyloxy)-phenyl)-amineHCID 21952074—

Reaction Steps

(6-Chloropyrido[3,4-d]pyrimidin-4-yl)-(4-(3-fluorobenzyloxy)-phenyl)-amine (1.85 g) and 5-(1,3-dioxolan-2-yl)-2-(tributylstannyl)-furan (3.82 g) in dioxan (40 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 (1.74 g); m/z 485 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713485B2
Source datasetuspto-grants-2004_03
ORD IDord-d877b9e943e84bc1bcf3ecd3a5d133f1
Source noteuspto-grants-2004_03