Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435193Generated: November 2, 2026

5-Pyrimidinecarboxamide, 4-amino-2-(ethylthio)-N-methoxy-N-methyl- → HCID 11722738, compound

https://huagongshe.com/reaction/1435193

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Pyrimidinecarboxamide, 4-amino-2-(ethylthio)-N-methoxy-N-methyl-HCID 11974832—
ReactantHCID 178506745HCID 178506745—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11722738HCID 11722738—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 4-amino-2-ethylsulfanyl-pyrimidine-5-carboxylic acid methoxy-methylamide (400 mg, 1.65 mmol, Example 1) was dissolved in anhydrous tetrahydrofuran (6 mL) and cooled to −78° C. A solution of the freshly prepared 2-methoxyl-5-fluorophenyl lithium (˜5 equiv, prepared following the same procedure as described in Step A of Example 2) was added over 10-30 minutes and the orange colored reaction mixture was stirred at −78 to 0° C. for 1-3 hours until the complete consumption of the starting material. The resulting mixture was quenched with aqueous ammonium chloride solution, 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 80/20→60/40 of hexane/ethyl acetate to give (4-amino-2-ethylsulfanyl-pyrimidin-5-yl)-(5-fluoro-2-methoxy-phenyl)-methanone as a white solid (277 mg). MS (M+H)+, 308.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615634B2
Source datasetuspto-grants-2009_11
ORD IDord-d01b543008e7406fbc99d5f52bd30ea5
Source noteuspto-grants-2009_11