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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371591Generated: October 25, 2026

4-Amino-2-ethylsulfanylpyrimidine-5-carboxylic acid methoxymethylamide → HCID 10039812, compound

https://huagongshe.com/reaction/1371591

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-2-ethylsulfanylpyrimidine-5-carboxylic acid methoxymethylamideHCID 10105787—
ReactantHCID 178506687HCID 178506687—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10039812HCID 1003981294%

Reaction Conditions

Temperature-78 °C

Reaction Steps

4-Amino-2-ethylsulfanylpyrimidine-5-carboxylic acid methoxymethylamide (200 mg, 0.830 mmol, Example 1) was dissolved in anhydrous tetrahydrofuran (3 mL) and cooled to −78° C. A solution of 2-methoxyphenyl lithium (˜3 equiv, freshly prepared following the same procedure as Step A of Example 2) was added. The reaction was stirred at −78° C. for 1.5 hours and quenched with aqueous ammonium chloride solution. The resulting mixture was extracted with ethyl acetate (3×20 mL), washed with brine (2×10 mL), dried over sodium sulfate and evaporated in vacuo. The residue was purified on silica gel with 60:40 of hexane/ethyl acetate to give (4-amino-2-ethylsulfanylpyrimidin-5-yl)-(2-methoxy-phenyl)-methanone as a white solid (224.1 mg, 94% yield). HRMS, observed: 290.0961; Calcd for (M+H)+: 290.0958.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157455B2
Source datasetuspto-grants-2007_01
ORD IDord-fa434ec979424feeb15a69d7fbb27939
Source noteuspto-grants-2007_01