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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086978Generated: November 1, 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-(4-fluorobenzyloxy)-phenyl)-amine

https://huagongshe.com/reaction/2086978

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-(4-fluorobenzyloxy)-phenyl)-amineHCID 21952330—
Solvent1,4-DioxaneHCID 31275—
Product(6-(5-(1,3-Dioxolan-2-yl)-furan-2-yl)-pyrido[3,4-d]pyrimidin-4-yl)-(4-(4-fluorobenzyloxy)-phenyl)-amineHCID 21952264—

Reaction Steps

(6-Chloropyrido[3,4-d]pyrimidin-4-yl)-(4-(4-fluorobenzyloxy)-phenyl)-amine (1.82 g) and 5-(1,3-dioxolan-2-yl)-2-(tributylstannyl)-furan (3.75 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 (1.21 g); m/z 485 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06727256B1
Source datasetuspto-grants-2004_04
ORD IDord-d6d494a0075e4185b5a350738fd0de65
Source noteuspto-grants-2004_04