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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 379980생성일: 2026년 10월 24일

Sodium Carbonate → HCID 20692737, 화합물

https://huagongshe.com/ko/reaction/379980

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-(3-bromophenyl)-N-methylacetamideHCID 18668529—
반응물(1S,2R)-4-[2-(tert-butyldimethylsilanyloxy)-1-methyl-4-pyridin-3-ylbutoxy]benzeneboronic acidHCID 54020751—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
용매TolueneHCID 1140—
생성물HCID 20692737HCID 2069273777%

반응 단계

A solution of (1S,2R)-4-[2-(tert-butyldimethylsilanyloxy)-1-methyl-4-pyridin-3-ylbutoxy]benzeneboronic acid (0.20 g, Example 11), 2-(3-bromophenyl)-N-methyl -acetamide (0.21 g, Example 12a)), 2M aqueous sodium carbonate (0.57 ml) and tetrakis(triphenylphosphine)palladium (0) (0.1 g) in toluene (5 ml) and ethanol (2 ml) was heated at 100° C. for 4 hours. After cooling, the solution was concentrated under reduced pressure. Concentrated hydrochloric acid (1 ml) was added to a solution of the residue in methanol (5 ml). The suspension was stirred at room temperature for 18 hours. The mixture was concentrated under reduced pressure and the residue partitioned between ether and water. The aqueous layer was neutralised and extracted with dichloromethane (2×50 ml). The combined extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by normal-phase HPLC eluting with a gradient of 0-25% ethanol in dichloromethane to give the title compound as an oil (0.15 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06300352B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-3598a98110e447a9b81a5785a84888de
출처 메모uspto-grants-2001_10