تفاعل #416850

ord-3c5cf040a81944f78561520ea6ce12fc

معادلة التفاعل

O=C(OCc1ccc([N+](=O)[O-])cc1)C1=C(n2cc(CCO)nn2)C[C@@H]2CC(=O)N12
p-nitrobenzyl 2-(4-[2-hydroxyethyl]-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylate
O=S(=O)(O)CCCN1CCOCC1
4-morpholinepropanesulfonic acid
O=C(O)C1=C(n2cc(CCO)nn2)C[C@@H]2CC(=O)N12
2-(4-[2-hydroxyethyl]-1,2,3-triazol-1-yl)-carbapen-2-em-3-carboxylic acid

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلthe pellet washed with deionized water (3×0.5 ml)
  2. 2
    استخلاصThe combined supernate and washes were extracted with ethyl acetate (3×0.5 ml)
  3. 3
    تركيزconcentrated under vacuum

الإجراء التجريبي

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-[2-hydroxyethyl]-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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04892869uspto-grants-1990_01