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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 847199생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/847199

반응식

참여 물질

역할이름HCID투입량
반응물MopsHCID 70807—
반응물p-Nitrobenzyl 2-(4-[2-hydroxyethyl]-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylateHCID 131715747—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물2-(4-[2Hydroxyethyl]-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylic acidHCID 131715746—

반응 단계

A solution of p-nitrobenzyl 2-(4-[2-hydroxyethyl]-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylate (3.5 mg, 8.8 micromol) in dioxane (300 microliter), deionized water (180 microliter), absolute ethanol (24 microliter), and pH 7.0 4-morpholinepropanesulfonic acid buffer (60 microliter of 0.5M) was shaken with 10% (w/w) palladium on charcoal (7.0 mg) under hydrogen (50 psig) at ambient temperature. After 40 min. the mixture was centrifuged and the pellet washed with deionized water (3×0.5 ml). The combined supernate and washes were extracted with ethyl acetate (3×0.5 ml) and concentrated under vacuum to provide 0.5 ml of a solution of 2-(4-[2hydroxyethyl]-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylic acid, UV λmax 299 nm which quenched upon addition of hydroxylamine hydrochloride and dipotassium hydrogen phosphate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05140030
출처 데이터셋uspto-grants-1992_08
ORD IDord-c0e41c04accb4c17b5c9fae0c235599f
출처 메모uspto-grants-1992_08