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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 222585생성일: 2026년 10월 25일

Methanol → 2-methyl-1-[4-[[6-(1-methylsulfonyl-3,6-dihydro-2H-pyridin-4-yl)-3-pyridyl]oxymethyl]-1-piperidyl]propan-2-ol

https://huagongshe.com/reaction/222585

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물2-Butylene oxideHCID 18632—
반응물4-(1'-Methanesulfonyl-1',2',3',6'-tetrahydro-[2,4']bipyridinyl-5-yloxymethyl)-piperidineHCID 66864837—
생성물2-methyl-1-[4-[[6-(1-methylsulfonyl-3,6-dihydro-2H-pyridin-4-yl)-3-pyridyl]oxymethyl]-1-piperidyl]propan-2-olHCID 66864747—

반응 단계

4-(1′-Methanesulfonyl-1′,2′,3′,6′-tetrahydro-[2,4′]bipyridinyl-5-yloxymethyl)-piperidine is suspended in 800 mL of methanol and added to an autoclave with a mechanical stirrer. 1500 mL of methanol are added and then dimethyloxirane (117 g, 1.62 mol) is added. The mixture is stirred at 60˜70° C. for 88 h, cooled to 25˜30° C. and concentrated to 1000 mL. The mixture is heated at 60˜70° C. and 4200 mL of water are added. The resulting mixture is stirred at 60˜70° C. during 30 min and cooled slowly to 0˜5° C. in 1.5˜2 h. It is stirred at this temperature for 30 minutes and filtered. The cake is slurried with H2O: MeOH=3:1 (600 mL) pre-cooled to 0˜5° C. and concentrated (2×). The product is dried under vacuum at 40˜50° C. to provide 320 g of off-white solid with 98.3% HPLC purity.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207344B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-ff3ed466ecfd4a24845038160a411a61
출처 메모uspto-grants-2012_06