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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234879Generated: October 27, 2026

2-Acetylthiophene → 2-Methyl-7-(2-thienyl)-pyrido[2,3-d]pyrimidine

https://huagongshe.com/reaction/234879

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AcetylthiopheneHCID 6920—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Amino-2-methylpyrimidine-5-carbaldehydeHCID 12904726—
SolventMethanolHCID 887—
Product2-Methyl-7-(2-thienyl)-pyrido[2,3-d]pyrimidineHCID 2335310417%

Reaction Steps

1 ml of 40% strength by weight aqueous potassium hydroxide solution was added to a suspension of 2.0 g (14.6 mmol) of 4-amino-5-formyl-2-methylpyrimidine and 1.93 g. (15.3 mmol) of 2-acetylthiophene in 25 ml of methanol. The reaction mixture was then stirred for 20 hours at 20°-25° C. after which the solvent was removed After the residue had been taken up in dichloromethane, the organic phase was washed with water, dried and evaporated down. Yield: 17%; mp.: 175°-180° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597776
Source datasetuspto-grants-1997_01
ORD IDord-7a9f5c9d3ce34332972a7aa089723b7c
Source noteuspto-grants-1997_01