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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329684생성일: 2026년 10월 25일

18-Crown-6 → 1-{[4-(2,3-Dichlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyrid-2-yl]methoxy}-2-hydroxy-2-methyl-3-(1,2,4-triazol-1-yl)propane

https://huagongshe.com/reaction/329684

반응식

참여 물질

역할이름HCID투입량
반응물18-Crown-6HCID 28557—
반응물2-{[4-(2,3-Dichlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyrid-2-yl]methoxymethyl}-2-methyloxiraneHCID 14810596—
반응물1h-1,2,4-Triazole sodium saltHCID 45489822—
용매TetrahydrofuranHCID 8028—
생성물1-{[4-(2,3-Dichlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyrid-2-yl]methoxy}-2-hydroxy-2-methyl-3-(1,2,4-triazol-1-yl)propaneHCID 2014767553.4%

반응 단계

A mixture of 2-{[4-(2,3-dichlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyrid-2-yl]methoxymethyl}-2-methyloxirane (0.80 g), 1,2,4-triazole sodium salt (0.60 g) and "18-Crown-6" (20 mg) in tetrahydrofuran (25 ml) was stirred at room temperature for two days and then partitioned between ethyl acetate and water. The layers were separated and the organic layer was washed with water, dried over Na2SO4 and evaporated. The residue was purified by chromatography on SiO2 (12 g) using toluene plus 0-100% ethyl acetate as the eluant. Appropriate fractions were combined and evaporated and the residue was triturated with ether. The resulting solid was collected, washed with ether and dried to give the title compound (0.49 g), m.p. 149°-160° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04892881
출처 데이터셋uspto-grants-1990_01
ORD IDord-443e1c0bd65a4e88a3a84096de3ab4e7
출처 메모uspto-grants-1990_01