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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1450151생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물PyridineHCID 1049—
반응물2-Fluoro-4-methylpyridin-3-amineHCID 2763161—
반응물6-Bromo-2-chlorosulfonyl-8-methoxy[1,2,4]triazolo[1,5-a]pyrazineHCID 19975236—
용매AcetonitrileHCID 6342—
생성물N-(2-Fluoro-4-methyl-3-pyridinyl)-6-bromo-8-methoxy[1,2,4]triazolo[1,5-a]pyrazine-2-sulfonamideHCID 19975246—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05602075
출처 데이터셋uspto-grants-1997_02
ORD IDord-c34e634c2e454d3a9d50c5dd0ec0e4f1
출처 메모uspto-grants-1997_02