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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2231699생성일: 2026년 10월 25일

Mops → 2-(4-Methyl-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylic acid

https://huagongshe.com/reaction/2231699

반응식

참여 물질

역할이름HCID투입량
반응물MopsHCID 70807—
반응물p-Nitrobenzyl 2-(4-methyl-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylateHCID 131715753—
반응물p-Nitrobenzyl 2-(5-methyl-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylateHCID 131715754—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물2-(4-Methyl-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylic acidHCID 131715751—
생성물2-(5-Methyl-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylic acidHCID 131715752—

반응 단계

A solution of a mixture of p-nitrobenzyl 2-(4-methyl-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylate and p-nitrobenzyl 2-(5-methyl-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylate (0.7 mg) in dioxane (100 microliter), deionized water (60 microliter), absolute ethanol (8.3 microliter), and pH 7.0 0.5M aqueous 4-morpholinepropanesulfonic acid (10.2 microliter) was shaken with 10% (w/w) palladium on charcoal (1.0 mg) under hydrogen (50 psig) at ambient temperature. After 30 min. the mixture was centrifuged and the pellet was washed with deionized water (5×0.5 ml). The combined supernate and washes were extracted with ethyl acetate (3×0.5 ml) and concentrated under vacuum at 0° C. to provide 2.0 ml of a solution of 2-(4-methyl-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylic acid and 2-(5-methyl-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylic acid, UV λmax 295 nm quenched by addition of hydroxylamine hydrochloride and dipotassium hydrogen phosphate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04783453
출처 데이터셋uspto-grants-1988_11
ORD IDord-d6beba4ecefd412c8a23437a02da5322
출처 메모uspto-grants-1988_11