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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 241673생성일: 2026년 10월 25일

Hydrogen Peroxide → (R)-tert-butyl 3-(1-(2-(dimethylamino)ethyl)-2-neopentyl-1H-benzo[d]imidazol-5-ylsulfonyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/241673

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물WaterHCID 962—
반응물Methanesulfonic AcidHCID 6395—
반응물Sodium ThiosulfateHCID 24477—
반응물Sodium BicarbonateHCID 516892—
반응물(R)-tert-butyl 3-(1-(2-(dimethylamino)ethyl)-2-neopentyl-1H-benzo[d]imidazol-5-ylthio)pyrrolidine-1-carboxylateHCID 58513598—
촉매Sodium Tungstate DihydrateHCID 150191—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물(R)-tert-butyl 3-(1-(2-(dimethylamino)ethyl)-2-neopentyl-1H-benzo[d]imidazol-5-ylsulfonyl)pyrrolidine-1-carboxylateHCID 5851360471%

반응 단계

To a solution of (R)-tert-butyl 3-(1-(2-(dimethylamino)ethyl)-2-neopentyl-1H-benzo[d]imidazol-5-ylthio)pyrrolidine-1-carboxylate (STEP A, 802 mg, 1.74 mmol) in methanol (15 mL) was added methane-sulfonic acid (226 microL, 3.46 mmol), 30% hydrogen peroxide solution (622 microL, 6.09 mmol) and sodium tungstate dihydrate (28.7 mg, 0.0870 mmol) in water solution (0.5 mL) at 0° C. The resulting solution was stirred at room temperature for 5 h. The reaction mixture was added sodium thiosulfate aqueous solution and sodium bicarbonate aqueous solution and diluted with dichloromethane to separate. The organic layer was concentrated in vacuo. The residue was purified by amine gel column chromatography (hexane-ethyl acetate, gradient) to give the title compound (612 mg, 71%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653063B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-11c93fff80824fdea864bcd3180bb5a7
출처 메모uspto-grants-2014_02