Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085948Generated: October 26, 2026

2-(Tributylstannyl)furan → (1-Benzyl-1H-indazol-5-yl)-(pyrido[3,4-d]pyrimidin-4-yl)-amine

https://huagongshe.com/reaction/2085948

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)furanHCID 4393688—
Reactant(1-Benzyl-1H-indazol-5-yl)-(6-chloropyrido[3,4-d]pyrimidin-4-yl)-amineHCID 21952012—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
Solvent1,4-DioxaneHCID 31275—
Product(1-Benzyl-1H-indazol-5-yl)-(pyrido[3,4-d]pyrimidin-4-yl)-amineHCID 22727452—

Reaction Steps

A stirred solution of (1-Benzyl-1H-indazol-5-yl)-(6-chloro-pyrido[3,4-d]pyrimidin-4-yl)-amine (0.165 g), 2-(tri-n-butylstannyl)furan (0.139 g) and bis-(triphenylphosphine)palladium (II) chloride (30 mg) in dioxane (10 ml) was heated at reflux under nitrogen for 65 hr (Procedure B). The cooled mixture was absorbed onto silica and chromatographed to give the title compound as an orange solid; δH CDCl3 9.34(1H,s), 8.82(1H,s), 8.70(1H,d), 8.15(1H,d), 8.10(1H,s), 7.65(1H,d), 7.60(1H,s), 7.53(1H,dd), 7.40(1H,d), 7.25(6H,m), 5.60(2H,s); m/z (M+1)+353.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06723726B1
Source datasetuspto-grants-2004_04
ORD IDord-e59afd2561f042e59e757034c1f2ec2e
Source noteuspto-grants-2004_04