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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 579575생성일: 2026년 10월 25일

Tetrahydrofuran → 2-acetamido-N-tert-butyl-2-((R)-1-(4-fluorobenzyl)pyrrolidin-3-yl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanamide

https://huagongshe.com/reaction/579575

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물1,2-Bis(diphenylphosphino)ethaneHCID 74267—
반응물4,4,5,5-Tetramethyl[1,3,2]dioxaborolaneHCID 2734768—
반응물HCID 66832976HCID 66832976—
촉매Chloro(1,5-cyclooctadiene)iridium(I) dimerHCID 6436381—
용매Sodium BicarbonateHCID 516892—
생성물2-acetamido-N-tert-butyl-2-((R)-1-(4-fluorobenzyl)pyrrolidin-3-yl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanamideHCID 66833480—

반응 조건

온도0 °C

반응 단계

A solution of bis(1,5-cyclooctadiene)diiridium(I) dichloride (35.0 mg, 0.0520 mmol) and 1,2-bis(diphenylphosphino)-ethane (44 mg, 0.11 mmol) in tetrahydrofuran (5 mL, 60 mmol) was cooled to 0° C. After stirring for 10 min 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (120 uL, 0.83 mmol) was added in a single portion via syringe and the reaction mixture was stirred at 0° C. for 5 min before warming to room temperature and stirring an additional 15 min. The reaction mixture was recooled to 0° C. and treated with 2-acetamido-N-tert-butyl-2-[(3R)-1-(4-fluorobenzyl)pyrrolidin-3-yl]hex-5-enamide (210 mg, 0.52 mmol) in tetrahydrofuran (3 mL, 40 mmol) in a single portion. After stirring for 10 min at 0° C., the reaction was warmed to room temperature and stirred an additional 4 h. The mixture was diluted with aqueous sodium bicarbonate, extracted with DCM (3×50 mL), dried over Na2SO4, filtered and concentrated to give 2-acetamido-N-tert-butyl-2-((R)-1-(4-fluorobenzyl)pyrrolidin-3-yl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanamide as a light orange oil that was used without further purification. ESI MS found for C29H47BFN3O4 m/z 532.3 (M+H)+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09040703B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-636fe8cc04b74899b11fd1b776eaa443
출처 메모uspto-grants-2015_05