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HRID 329671作成日:2026年10月25日

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

https://huagongshe.com/reaction/329671

反応式

関与物質

役割名称HCID仕込み量
反応物MopsHCID 70807—
反応物p-Nitrobenzyl 2-(4-methyl-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylateHCID 131715753—
反応物p-Nitrobenzyl 2-(5-methyl-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylateHCID 131715754—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物2-(4-Methyl-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylic acidHCID 131715751—
生成物2-(5-Methyl-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylic acidHCID 131715752—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04892869
出典データセットuspto-grants-1990_01
ORD IDord-44eff9adb1504adc87d45d509816fadc
出典メモuspto-grants-1990_01