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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626354Generated: November 4, 2026

Methyl iodide → HCID 56960510, compound

https://huagongshe.com/reaction/1626354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 118249754HCID 118249754—
SolventDimethylacetamideHCID 31374—
ProductHCID 56960510HCID 5696051097.1%

Reaction Conditions

Temperature27 °C

Reaction Steps

To a solution (Z)-ethyl 4-((6-(3-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)-5-methylpyrimidin-4-yl)oxy)piperidine-1-carboxylate (300 mg, 0.0006198 mole) in dimethyl acetamide (10 ml), K2CO3 (171 mg, 0.001239 mole) was added followed by addition of methyl iodide (0.060 ml, 0.0009297 mole) at 0° C. and reaction mixture was stirred at 27° C. for 30 minutes. Then reaction mixture was poured into ice cold water and extracted with ethyl acetate. Organic layer was washed with water and brine, dried over sodium sulfate and evaporated on a rotavpour to yield the product as yellow solid (300 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785463B2
Source datasetuspto-grants-2014_07
ORD IDord-2676d09d4b74401daa3162514a4e2f41
Source noteuspto-grants-2014_07