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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46205생성일: 2026년 10월 24일

Sodium hydride → 2-(2-Chloro-5-((2S,3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)phenyl)(6-chloropyridazin-3-yl)methanone

https://huagongshe.com/ko/reaction/46205

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물DimethylacetamideHCID 31374—
반응물3,6-DichloropyridazineHCID 67331—
반응물(2S,3R,4R,5S,6R)-2-(4-Chloro-3-((5-(methylthio)-1,3,4-thiadiazol-2-yl)methyl)phenyl)-6-(hydroxymethyl)-tetrahydro-2H-pyran-3,4,5-triolHCID 46229266—
반응물2-(2-Chloro-5-((3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)phenyl)acetonitrileHCID 67287790—
생성물2-(2-Chloro-5-((2S,3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)phenyl)(6-chloropyridazin-3-yl)methanoneHCID 86664429—

반응 조건

온도0 °C

반응 단계

Sodium hydride (593 mg; 14.8 mmol; 60% in mineral oil) was added to stirred solution of Intermediate 1 (compound 6, 5.00 g; 7.42 mmol) in 20 mL of N,N-dimethylacetamide (DME) at 0° C. under nitrogen gas. The reaction mixture was stirred for 30 min, and 3,6-dichloropyridazine (compound 22, 1.25 g; 8.16 mmol) was added in one portion. The ice bath was removed, and the reaction mixture was stirred at room temperature for 3.5 h. Cooled to 0° C., H2O2 (2.50 mL) was added to reaction mixture and left stirring additional hour warm-up to room temperature. The reaction solution was washed with 1N HCl solution, 1N NaOH solution and brine. The organic layer was collected, and evaporated under a vacuum. The crude mixture was further purified by flash column chromatography (Biotage SP1™) to obtain 3.10 g (4.00 mmol; 54%) of the title compound as orange oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541380B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-86014667753642a695508f002b398cac
출처 메모uspto-grants-2013_09