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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252726Generated: October 26, 2026

Citric Acid → Propane-1-sulfonic acid {6-[2-(5-methoxy-pyrimidin-2-yloxy)-ethoxy]-5-p-tolyl-pyrimidin-4-yl}-amide

https://huagongshe.com/reaction/2252726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantSodium hydrideHCID 24758—
Reactant2-Methanesulfonyl-5-methoxy-pyrimidineHCID 4159151—
Reactantn-Propanesulfonic acid [6-(2-hydroxy-ethoxy)-5-p-tolyl-pyrimidin-4-yl]-amideHCID 86597591—
SolventTetrahydrofuranHCID 8028—
ProductPropane-1-sulfonic acid {6-[2-(5-methoxy-pyrimidin-2-yloxy)-ethoxy]-5-p-tolyl-pyrimidin-4-yl}-amideHCID 5964526740.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

n-Propanesulfonic acid [6-(2-hydroxy-ethoxy)-5-p-tolyl-pyrimidin-4-yl]-amide (115.5 mg) was dissolved in THF (10 ml) and sodium hydride (60 mg) was added followed by stirring for 15 min at 50° C. Then 2-methanesulfonyl-5-methoxy-pyrimidine (138 mg) was added and stirring was continued for 8 h at 75° C. The reaction mixture was poured onto ice water, acidified with solid citric acid and extracted with ethyl acetate. The combined organic layers were dried over magnesium sulfate and the solvent was evaporated. The crude material was purified by plate chromatography with diethyl ether to give propane-1-sulfonic acid {6-[2-(5-methoxy-pyrimidin-2-yloxy)-ethoxy]-5-p-tolyl-pyrimidin-4-yl}-amide (61 mg) as a white powder. LC-MS: tR: 4.51, [M+H]+: 460.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323465B2
Source datasetuspto-grants-2008_01
ORD IDord-c9387b5c9d1d46d4bfd88d7ad5e573c6
Source noteuspto-grants-2008_01