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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579252Generated: November 3, 2026

Methyl iodide → 58536-95-1

https://huagongshe.com/reaction/1579252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1-[(4-fluorophenyl)methyl]-2-(methylamino)-1H,4H-pyrido[2,3-d]pyrimidin-4-oneHCID 4067058—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product58536-95-1HCID 5072574—

Reaction Steps

To a suspension of 10.0 g. of powdered 1-(4'-fluorobenzyl)-2-methylamino-pyrido[2,3-d]pyrimidin-4(1H)-one in 300 ml. of tetrahydrofuran is added portionwise over the course of 5 minutes 4.8 g. of potassium t-butoxide and the resulting mixture is stirred at room temperature for 45 minutes. There is then added 6.5 g. of methyl iodide followed by stirring at room temperature for two days. The resulting mixture is filtered through celite and the filtrate evaporated to dryness. The residue is dissolved in 100 ml. of methylene chloride, washed twice with water, dried, filtered and evaporated to dryness. The residue is dissolved in a small amount of chloroform and filtered through a 650 ml. filter column using silica and chloroform. The combined product containing fractions are evaporated to dryness, the residue dissolved in 50 ml. of methylene chloride and ether added while warming on a steam bath to obtain 1-(4'-fluorobenzyl)-2-dimethylamino-pyrido[2,3-d]pyrimidin-4(1H)-one, m.p. 167°-170°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931183
Source datasetuspto-grants-1976_01
ORD IDord-36ce0b2f672a4a389964b5c7bd4909b0
Source noteuspto-grants-1976_01