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HRID 1450151作成日:2026年10月27日

Dimethyl Sulfoxide → N-(2-Fluoro-4-methyl-3-pyridinyl)-6-bromo-8-methoxy[1,2,4]triazolo[1,5-a]pyrazine-2-sulfonamide

https://huagongshe.com/reaction/1450151

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物PyridineHCID 1049—
反応物2-Fluoro-4-methylpyridin-3-amineHCID 2763161—
反応物6-Bromo-2-chlorosulfonyl-8-methoxy[1,2,4]triazolo[1,5-a]pyrazineHCID 19975236—
溶媒AcetonitrileHCID 6342—
生成物N-(2-Fluoro-4-methyl-3-pyridinyl)-6-bromo-8-methoxy[1,2,4]triazolo[1,5-a]pyrazine-2-sulfonamideHCID 19975246—

反応手順

A solution of 1.36 g (4.14 mmol) of 6-bromo-2-chlorosulfonyl-8-methoxy[1,2,4]triazolo[1,5-a]pyrazine in 15 mL of dry acetonitrile was placed in a flask equipped with a drying tube and was treated sequentially with 1.56 g (12.4 mmol) of 3-amino-2-fluoro-4-methylpyridine, 0.34 mL (4.21 mmol) of pyridine and 60 μL (0.85 mmol) of dimethyl sulfoxide at room temperature. The reaction became progressively darker and after 15 hours the volatiles were removed by evaporation under reduced pressure and the residue was dissolved in dichloromethane. The resulting solution was washed with four portions of 1M hydrochloric acid and one portion of water and was dried over sodium sulfate. The solvent was then removed by evaporation under reduced pressure and the residue obtained was purified by flash column chromatography on silica gel using a 0.5 to 4 percent ethanol/dichloromethane gradient as eluent. The solid obtained was further purified by extraction with diethyl ether to obtain 373 mg (22 percent of theory) of the desired product as an off-white powder melting at 210°-211° C. (dec); Mass Spectrum, m/e 417 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05602075
出典データセットuspto-grants-1997_02
ORD IDord-c34e634c2e454d3a9d50c5dd0ec0e4f1
出典メモuspto-grants-1997_02