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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1975604생성일: 2026년 10월 26일

Dicyclohexylcarbodiimide → 6-(1-Imidazolylmethyl)benzoxazol-2-yl-methyl methyl 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate

https://huagongshe.com/reaction/1975604

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물2,6-Dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid monomethyl esterHCID 173322—
반응물2-Hydroxymethyl-6-(1-imidazolylmethyl)benzoxazoleHCID 70047035—
용매TolueneHCID 1140—
생성물6-(1-Imidazolylmethyl)benzoxazol-2-yl-methyl methyl 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylateHCID 70048044—

반응 단계

332 mg (1 mM) of 1,4-dihydro-2,6-dimethyl-5-methoxycarbonyl-4-(3-nitrophenyl)pyridine-3-carboxylic acid together with 229 mg (1 mM) of 2-hydroxymethyl-6-(1-imidazolylmethyl)benzoxazole 248 mg (1.2 mM) of dicyclohexylcarbodiimide and 134 mg (1.1 mM) of 4-N,N-dimethylaminopyridine were dissolved in 5 ml of toluene, while heating, and refluxed for six hours. The solution was cooled to room temperature, and the crystals produced were filtered off. The filtrate was washed with water and dried over anhydrous sodium sulfate. After the solvent was distilled off, the residue was purified by chromatography on a silica gel column, whereby the captioned compound was obtained. The yield was 542 mg (99.9%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05286869
출처 데이터셋uspto-grants-1994_02
ORD IDord-226a9f9367aa4ac39fbe3ddc55086a66
출처 메모uspto-grants-1994_02