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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096362Generated: October 31, 2026

Methyl iodide → 6-(6-chloro-2-methyl-pyrimidine-4-carbonyl)-3,4-dimethyl-3H-benzoxazol-2-one

https://huagongshe.com/reaction/2096362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant6-(6-chloro-2-methyl-pyrimidine-4-carbonyl)-4-methyl-3H-benzoxazol-2-oneHCID 58181118—
SolventDimethylformamideHCID 6228—
Product6-(6-chloro-2-methyl-pyrimidine-4-carbonyl)-3,4-dimethyl-3H-benzoxazol-2-oneHCID 58181137—

Reaction Steps

59 mg (1.4 mmol) sodium hydride (55%, suspension in mineral oil) were added at RT to 0.37 g (1.2 mmol) 6-(6-chloro-2-methyl-pyrimidin-4-carbonyl)-4-methyl-3H-benzoxazol-2-one in 5.0 mL. DMF. The reaction mixture was stirred for 30 min at RT. Then 0.10 ml. (1.60 mmol) iodomethane were added and the mixture was stirred for 1 h at RT. Then another 0.10 ml. (1.60 mmol) iodomethane were added and the mixture was stirred overnight at RT. The reaction mixture was diluted with ice water and the precipitate formed was suction filtered. The residue was washed with water and dried i. vac.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450327B2
Source datasetuspto-grants-2013_05
ORD IDord-861d6fbacb7f419e87ba631b1f87d77a
Source noteuspto-grants-2013_05