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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426266Generated: October 26, 2026

Potassium Carbonate → 3-[3-(2-Fluoro-5-nitro-pyridin-3-ylmethyl)-5-isopropyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidine-4-carbonyl]-5-methyl-benzonitrile

https://huagongshe.com/reaction/426266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantLithium iodideHCID 66321—
Reactant3-(5-Isopropyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidine-4-carbonyl)-5-methyl-benzonitrileHCID 46880377—
Reactant3-Bromomethyl-2-fluoro-5-nitro-pyridineHCID 59686862—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-[3-(2-Fluoro-5-nitro-pyridin-3-ylmethyl)-5-isopropyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidine-4-carbonyl]-5-methyl-benzonitrileHCID 5918470934.4%

Reaction Steps

3-(5-Isopropyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidine-4-carbonyl)-5-methyl-benzonitrile (37 mg, 0.124 mmol, 1.2 eq.) was dissolved in 1.5 mL DMF. Potassium carbonate (14 mg, 1 eq.) was added and the reaction was stirred at room temperature for 10 minutes. 3-Bromomethyl-2-fluoro-5-nitro-pyridine (27 mg, 0.103 mmol, 1 eq.) and lithium iodide (14 mg, 1 eq.) were added. The reaction was stirred at room temperature for 2 hours. Ethyl acetate was added to the reaction mixture, followed by washing with brine. The organic layer was concentrated down and purified (silica gel, 0-80% EtOAC/hexane) to give white powder (16 mg, 34%). LC-MS shows 449.9 (M−1). 1H NMR (300 MHz, CDCl3): δ 8.98 (d, 2H), 8.48 (m, 1H), 7.98 (s, 1H), 7.93 (s, 1H), 7.78 (m, 2H), 5.08 (d, 1H), 4.56 (d, 1H), 2.50 (s, 3H), 2.22 (m, 1H), 1.22 (dd, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106064B2
Source datasetuspto-grants-2012_01
ORD IDord-1d45665ea9884023be4ca37bbc2fdb6a
Source noteuspto-grants-2012_01