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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436406Generated: October 31, 2026

Tetrahydrofuran → 1-(3-Iodophenyl)-3,4-dihydropyrido[2,3-d]pyrimidin-2(1H)-one

https://huagongshe.com/reaction/436406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 21452453HCID 21452453—
SolventAcetoneHCID 180—
Product1-(3-Iodophenyl)-3,4-dihydropyrido[2,3-d]pyrimidin-2(1H)-oneHCID 13259332—

Reaction Steps

To a solution of 3.3 g of 2-(m-iodoanilino)-3-aminomethylpyridine and 30 ml of dry tetrahydrofuran was added 3.2 g of N,N'-carbonyldiimidazole and the mixture was heated under reflux for 12 hours. After the reaction was complete, the solvent was removed from the reaction mixture by distillation under reduced pressure. The residue thus obtained was dissolved in acetone. The acetone solution was placed on a column of alumina and eluted with acetone. The eluate was concentrated and left to yield 2.5 g of 1-(m-iodophenyl)-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidine as colorless needles, melting at 175° - 177° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04009166
Source datasetuspto-grants-1977_02
ORD IDord-b160a19d7d28440c84a267054daef3b3
Source noteuspto-grants-1977_02