Alternatived Products of [ 5349-80-4 ]
Product Details of [ 5349-80-4 ]
CAS No. : | 5349-80-4 |
MDL No. : | MFCD00243727 |
Formula : |
C2H6N2O2
|
Boiling Point : |
- |
Linear Structure Formula : | - |
InChI Key : | - |
M.W : |
90.08
|
Pubchem ID : | - |
Synonyms : |
|
Application In Synthesis of [ 5349-80-4 ]
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
- Downstream synthetic route of [ 5349-80-4 ]
- 1
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[ 7790-86-5 ]
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[ 5349-80-4 ]
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[ 6046-93-1 ]
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[ 5743-47-5 ]
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C13H33CeClCu5N10O17(1+)*Cl(1-)
[ No CAS ]
- 2
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praseodymium(III) chloride
[ No CAS ]
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[ 5349-80-4 ]
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[ 6046-93-1 ]
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[ 5743-47-5 ]
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C13H33ClCu5N10O17Pr(1+)*Cl(1-)
[ No CAS ]
- 3
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neodymium(III) chloride
[ No CAS ]
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[ 5349-80-4 ]
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[ 6046-93-1 ]
-
[ 5743-47-5 ]
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C13H33ClCu5N10NdO17(1+)*Cl(1-)
[ No CAS ]
- 4
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samarium(III) chloride
[ No CAS ]
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[ 5349-80-4 ]
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[ 6046-93-1 ]
-
[ 5743-47-5 ]
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C13H33ClCu5N10O17Sm(1+)*Cl(1-)
[ No CAS ]
- 5
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europioum(III) chloride
[ No CAS ]
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[ 5349-80-4 ]
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[ 6046-93-1 ]
-
[ 5743-47-5 ]
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C13H33ClCu5EuN10O17(1+)*Cl(1-)
[ No CAS ]
- 6
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[ 5349-80-4 ]
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gadolinium(III) chloride hexahydrate
[ No CAS ]
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[ 6046-93-1 ]
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[ 5743-47-5 ]
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C13H33ClCu5GdN10O17(1+)*Cl(1-)
[ No CAS ]
- 7
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terbium(III) chloride
[ No CAS ]
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[ 5349-80-4 ]
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[ 6046-93-1 ]
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[ 5743-47-5 ]
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C13H33ClCu5N10O17Tb(1+)*Cl(1-)
[ No CAS ]
- 8
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dysprosium(III) chloride
[ No CAS ]
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[ 5349-80-4 ]
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[ 6046-93-1 ]
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[ 5743-47-5 ]
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C13H33ClCu5DyN10O17(1+)*Cl(1-)
[ No CAS ]
- 9
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lanthanum(III) chloride
[ No CAS ]
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[ 5349-80-4 ]
-
[ 6046-93-1 ]
-
[ 5743-47-5 ]
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C13H33ClCu5LaN10O17(1+)*Cl(1-)
[ No CAS ]
- 10
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yttrium(III) chloride
[ No CAS ]
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[ 5349-80-4 ]
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[ 6046-93-1 ]
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[ 5743-47-5 ]
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C13H33ClCu5N10O17Y(1+)*Cl(1-)
[ No CAS ]
- 11
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[ 464192-28-7 ]
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[ 5349-80-4 ]
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[ 18063-02-0 ]
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[2-(2-bromothiazol-5-yl)-3-(2,6-difluorobenzoyl)-5-oxoimidazolidin-1-yl] 2,6-difluorobenzoate
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
9% |
|
To a suspension of 2-aminoethanehydroxamic acid (Intermediate 1 , 36 mg, 0.40 mmol) in acetonitrile (1 mL) was added a solution of <strong>[464192-28-7]2-bromothiazole-5-carbaldehyde</strong> (41 mg, 0.42 mmol) in acetonitrile (0.7 mL). The reaction mixture was stirred for 1 h. at reflux and at room temperature o/n. The mixture was cooled on an ice-water bath to < 5 C and N,N- diisopropylethylamine (257 mu, 1.56 mmol) was added. Subsequently a solution of 2,6- difluorobenzoyl chloride (108 mu, 0.86 mmol) in acetonitrile (0.5 mL) was added dropwise keeping the temperature below 5 C. The temperature of the reaction mixture was allowed to come to room temperature. The mixture was diluted with ethyl acetate (5 mL) and water (3 mL) was added slowly. The resulting phases were separated and the water layer was extracted with ethyl acetate (3 mL). The combined organic layers were washed with water (5 mL), 5% NaHCCh- solution (5 mL), water (5 mL) and brine (5 mL), filtered over a PE filter filled with Na2S04 and concentrated under reduced pressure. The crude residue was purified by column chromatography (heptane to ethyl acetate = 0 to 100 v/v%) to afford the title compound (19 mg, 9%) as a white solid. |