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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654139Generated: November 3, 2026

Tributylstannane → HCID 178441857, compound

https://huagongshe.com/reaction/1654139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 178441862HCID 178441862—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 178441857HCID 178441857—

Reaction Steps

To a solution of 1.0 g of 2-butyl-1,4-dihydro-4-oxo-6-iodo-quinazoline and 0.355 g of tetrakis(triphenylphosphine)palladium in 15 ml of tetrahydrofuran and 5 ml of N,N-dimethylformamide, heated to 55° C. under an atmosphere of carbon monoxide is added a solution of 1.40 g of tri-n-butyltin hydride in 2.5 ml of toluene over 6 hours via a syringe pump. After the addition is complete the reaction is allowed to cool to room temperature, diluted with brine and extracted with chloroform. The combined organics are concentrated in vacuo and the resulting residue triturated with ether. The precipitate is collected by filtration and purified by flash chromatography on silica gel, eluting with 1:1 ethyl acetate-hexanes to give 0.35 g of the desired product, m.p. 242°-244° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05405849
Source datasetuspto-grants-1995_04
ORD IDord-d06c01f66a7a4e1c90542051f70ae2e2
Source noteuspto-grants-1995_04