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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436886Generated: November 3, 2026

Methyl iodide → HCID 69067168, compound

https://huagongshe.com/reaction/1436886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-oxo-2-[(pyrimidin-2-yl)methylamino]acetateHCID 69066482—
SolventDimethylformamideHCID 6228—
ProductHCID 69067168HCID 69067168—

Reaction Steps

A solution ethyl 2-oxo-2-[(pyrimidin-2-yl)methylamino]acetate from the previous step (1.0 g, 4.8 mmol) and iodomethane (0.5 mL, 8 mmol) in DMF (15 mL) was cooled to 0° C. and NaH (0.23 g of a 60% dispersion in mineral oil, 5.7 mmol) was added. The cooling bath was removed and the mixture was stirred at ambient temperature for 18 hours. Ethanol was added to quench the reaction and the solvent was removed under reduced pressure. The residue was purified by pressurized silica gel column chromatography using a gradient of 80-100% EtOAc in hexanes. The solvent was removed under reduced pressure from the fractions containing product to give the title compound as an oil. 1H NMR (400 MHz, DMSO-d6) δ 8.81 (m, 2H), 7.45 (m, 1H), 4.74 (m, 2H), 4.32, 4.13 (two q, rotamers, J=7 Hz, 2H), 3.08, 3.00 (two s, rotamers, 3H), 1.30, 1.08 (two t, rotamers, 3H); ES MS M+1=224.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07619086B2
Source datasetuspto-grants-2009_11
ORD IDord-c2acfbc5bdca469eb7c5b004ab577b52
Source noteuspto-grants-2009_11