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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51140Generated: October 28, 2026

2-(Tributylstannyl)furan-4-carboxaldehyde → 5-(4-(4-(3-Fluorobenzyloxy)-phenylamino)-pyrido[3,4-d]pyrimidin-6-yl)-furan-3-carbaldehyde

https://huagongshe.com/reaction/51140

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)furan-4-carboxaldehydeHCID 10959991—
Reactant(6-Chloropyrido[3,4-d]pyrimidin-4-yl)-(4-(3-fluorobenzyloxy)-phenyl)-amineHCID 21952062—
Solvent1,4-DioxaneHCID 31275—
Product5-(4-(4-(3-Fluorobenzyloxy)-phenylamino)-pyrido[3,4-d]pyrimidin-6-yl)-furan-3-carbaldehydeHCID 21952088—

Reaction Steps

(6-Chloropyrido[3,4-d]pyrimidin-4-yl)-(4-(3-fluorobenzyloxy)-phenyl)-amine (1 g) and 5-(tributylstannyl)-furan-3-carbaldehyde (J. Org. Chem. (1992), 57(11), 3126-31) (1.84 g) in dioxan (35 ml) were reacted together as in Procedure B. The solvent was evaporated and the residue suspended in dichloromethane. The mixture was filtered through Celite® and then evaporated. The residue was triturated with hexane giving a beige solid (1 g); m/z 441 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713485B2
Source datasetuspto-grants-2004_03
ORD IDord-a3818ff015a647a18eff43dbca56e84e
Source noteuspto-grants-2004_03