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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4665생성일: 2026년 10월 23일

Phenyl glycidyl ether → Dimethyl 4-[2-[4-(2-hydroxy-3-phenoxypropylamino)butoxy]-5-methylsulfonylphenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate

https://huagongshe.com/ko/reaction/4665

반응식

참여 물질

역할이름HCID투입량
반응물Phenyl glycidyl etherHCID 31217—
반응물Dimethyl 4-[2-(4-aminobutoxy)-5-methylsulfonylphenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylateHCID 14050493—
용매MethanolHCID 887—
생성물Dimethyl 4-[2-[4-(2-hydroxy-3-phenoxypropylamino)butoxy]-5-methylsulfonylphenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylateHCID 1405045030.9%

반응 단계

In 44 ml of methanol were dissolved 2.57 g of dimethyl 4-[2-(4-aminobutoxy)-5-methylsulfonylphenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate (obtained in Reference Example 2) and 0.83 g of glycidyl phenyl ether, and the solution formed was allowed to react at room temperature for 43 hours and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography, and the product was eluted with chloroform-methanol (95:5 v/v). Crude crystals were recrystallized from ethanol-ether to give 1.05 g of dimethyl 4-[2-[4-(2-hydroxy-3-phenoxypropylamino)butoxy]-5-methylsulfonylphenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727082
출처 데이터셋uspto-grants-1988_02
ORD IDord-95616be347ab446d930fbf2dcab17c14
출처 메모uspto-grants-1988_02