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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627497Generated: October 31, 2026

1,1'-Carbonyldiimidazole → N-Methoxy-N-methylpyrimidine-5-carboxamide

https://huagongshe.com/reaction/627497

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantPyrimidine-5-carboxylic acidHCID 78346—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventAmmonium ChlorideHCID 25517—
ProductN-Methoxy-N-methylpyrimidine-5-carboxamideHCID 66575045—

Reaction Steps

1,1′-carbonyldiimidazole (1.23 g, 7.57 mmol) was added to a suspension of pyrimidine-5-carboxylic acid (783 mg, 6.31 mmol) in DCM (20 mL) and the mixture was stirred at room temperature for 15 min before addition of N,O-dimethylhydroxylamine hydrochloride (739 mg, 7.57 mmol). The mixture was stirred at room temperature for 5 d, then was diluted with saturated aqueous NH4Cl and water and extracted with DCM. The organic phase was washed with water, and the aqueous phases were back-extracted with DCM. The organic phase was dried (Na2SO4), filtered, and concentrated, affording the crude title compound as a light yellow oil which was used without further purification in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309222B2
Source datasetuspto-grants-2016_04
ORD IDord-342d1264d4624837979f120d69c22553
Source noteuspto-grants-2016_04