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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 594150생성일: 2026년 10월 25일

1-Bromo-2-methylpropane → 4-{[(3,5-dimethyl-4-isoxazolyl)methyl]oxy}-N-(3,5-dimethyl-2-pyridinyl)-N-(2-methylpropyl)benzenesulfonamide

https://huagongshe.com/reaction/594150

반응식

참여 물질

역할이름HCID투입량
반응물1-Bromo-2-methylpropaneHCID 6555—
반응물2-tert-Butyl-1,1,3,3-tetramethylguanidineHCID 3571581—
반응물4-{[(3,5-dimethyl-4-isoxazolyl)methyl]oxy}-N-(3,5-dimethyl-2-pyridinyl)benzenesulfonamideHCID 89876385—
용매AcetonitrileHCID 6342—
생성물4-{[(3,5-dimethyl-4-isoxazolyl)methyl]oxy}-N-(3,5-dimethyl-2-pyridinyl)-N-(2-methylpropyl)benzenesulfonamideHCID 7219413746.6%

반응 단계

To a solution of 4-{[(3,5-dimethyl-4-isoxazolyl)methyl]oxy}-N-(3,5-dimethyl-2-pyridinyl)benzenesulfonamide (56 mg, 0.145 mmol) in acetonitrile (1 mL) was added N″-(1,1-dimethylethyl)-N,N,N′,N′-tetramethylguanidine (25 mg, 0.145 mmol) and the mixture was stirred at room temperature for 1 hour, 1-bromo-2-methylpropane (0.031 mL, 0.289 mmol) was then added and the mixture was stirred at 70° C. for 125 hours. The mixture was concentrated in vacuo and partitioned between dichloromethane (5 mL) and water (5 mL). The organic layer was then purified by mass directed autoprep (formic acid modifier) to give the title compound (30 mg) as a white solid. LCMS (2 min, formic) Rt 1.31 min, m/z (ES+) 444 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09242972B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-c2bc17e51b0d4e6f8d5cbd9ffc9d4aa7
출처 메모uspto-grants-2016_01