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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046307Generated: October 26, 2026

Triethylamine → (+/-)-4-Fluoro-2-methoxy-N-[1-(1-methyl-6-oxo-1,6-dihydro-[4,4']bipyrimidinyl-2-yl)-ethyl]-benzamide

https://huagongshe.com/reaction/2046307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiethyl cyanophosphonateHCID 76257—
Reactant4-Fluoro-2-methoxybenzoic acidHCID 2774545—
Reactant(+/-) 2-(1-amino-ethyl)-1-methyl-1H-[4,4']bipyrimidinyl-6-oneHCID 68527245—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product(+/-)-4-Fluoro-2-methoxy-N-[1-(1-methyl-6-oxo-1,6-dihydro-[4,4']bipyrimidinyl-2-yl)-ethyl]-benzamideHCID 2511621066%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 0.112 g (0.48 mmol) of (+/−) 2-(1-amino-ethyl)-1-methyl-1H-[4,4′]bipyrimidinyl-6-one in 5 mL of dimethylformamide was added 0.082 g (0.48 mmol) of 4-fluoro-2-methoxy-benzoic acid and 90 μL (0.58 mmol) of diethyl phosphorocyanidate (DEPC). The resulting mixture was cooled at 0° C., 70 μL (0.53 mmol) of triethylamine was added and stirred at room temperature for 1 h. Water was added and the mixture extracted with diethyl acetate. The extracts were washed with a saturated aqueous solution of ammonium chloride, dried and evaporated. The residue was purified on preparative thin layer chromatography eluting with a mixture of dichloromethane/methanol/aqueous ammonia solution (29%) in the proportions 95/5/0.5 to afford 0.12 g (66%) of the desired compound as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592436B2
Source datasetuspto-grants-2013_11
ORD IDord-18823f9eb1c84a8097cbd5a40db20c23
Source noteuspto-grants-2013_11