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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 594170생성일: 2026년 10월 27일

(Bromomethyl)cyclobutane → N-(cyclobutylmethyl)-4-((3,5-dimethylisoxazol-4-yl)methoxy)-N-(5-isopropylpyridin-2-yl)benzenesulfonamide

https://huagongshe.com/reaction/594170

반응식

참여 물질

역할이름HCID투입량
반응물(Bromomethyl)cyclobutaneHCID 2734658—
반응물2-tert-Butyl-1,1,3,3-tetramethylguanidineHCID 3571581—
반응물4-((3,5-dimethylisoxazol-4-yl)methoxy)-N-(5-isopropylpyridin-2-yl)benzenesulfonamideHCID 89876015—
용매AcetonitrileHCID 6342—
생성물N-(cyclobutylmethyl)-4-((3,5-dimethylisoxazol-4-yl)methoxy)-N-(5-isopropylpyridin-2-yl)benzenesulfonamideHCID 7219482223.9%

반응 조건

온도20 °C

반응 단계

To a solution of 4-((3,5-dimethylisoxazol-4-yl)methoxy)-N-(5-isopropylpyridin-2-yl)benzenesulfonamide (150 mg, 0.374 mmol) in acetonitrile (4 mL) stirred in air at 20° C., was added 2-(tert-butyl)-1,1,3,3-tetramethylguanidine (128 mg, 0.747 mmol). The reaction mixture was stirred at 20° C. for 1 hour, then (bromomethyl)cyclobutane (0.084 ml, 0.747 mmol) was added. The reaction was heated by microwaves to 150° C. for 30 minutes. After cooling the solvent was removed in vacuo and the residue was dissolved in ethyl acetate. The organic phase was washed with water (5 mL) and dried using a hydrophobic frit. The solvent was removed in vacuo to give the crude product as an orange oil. The crude product was purified by flash silica (Si) chromatography (0-25% ethyl acetate-cyclohexane gradient). The appropriate fractions were combined and evaporated in vacuo to give the title product (42 mg) as a colourless oil. LCMS (2 min, High pH) Rt 1.48 mins, m/z (ES+) 470, (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09242972B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-97324b61a9de49769aa3252483c0df8c
출처 메모uspto-grants-2016_01