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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405972Generated: October 30, 2026

Methyl iodide → HCID 58166486, compound

https://huagongshe.com/reaction/1405972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178425850HCID 178425850—
SolventDimethylformamideHCID 6228—
ProductHCID 58166486HCID 581664868%

Reaction Conditions

Temperature60 °C

Reaction Steps

To N-(5-fluoro-2-hydroxypyrimidin-4-yl)-4-methylbenzamide (200 mg, 0.81 mmol) in DMF (5 mL) was added K2CO3 (224 mg, 1.6 mmol), and iodomethane (230 mg, 1.6 mmol). The mixture was stirred and heated to 60° C. for 30 min and then stirred for 16 h at room temperature. The mixture was partitioned between ethyl acetate (EtOAc) and water (H2O). The organic phase was dried over magnesium sulfate (MgSO4), filtered and evaporated. The crude material was purified by reverse phase chromatography to yield the title compound as a white solid (17 mg, 8%): mp 229-230° C.; 1H NMR (300 MHz, CDCl3) δ13.2 (br s, 1H), 8.23-8.15 (br m, 2H), 7.42-7.37 (br m, 1H), 7.30-7.25 (br m, 2H), 3.45 (s, 3H), 2.44 (s, 3H); ESIMS m/z 262 ([M+H]+), m/z 260 ([M−H]−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916579B2
Source datasetuspto-grants-2014_12
ORD IDord-48978aa15dac4f93aa841e6cea05a52e
Source noteuspto-grants-2014_12