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Chemical Structure| 55152-01-7 Chemical Structure| 55152-01-7

Structure of 55152-01-7

Chemical Structure| 55152-01-7

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Product Details of [ 55152-01-7 ]

CAS No. :55152-01-7
Formula : C6H8N2O3
M.W : 156.13
SMILES Code : O=C(OC)CC1=NC(C)=NO1
English Name :Methyl 2-(3-methyl-1,2,4-oxadiazol-5-yl)acetate

Safety of [ 55152-01-7 ]

Application In Synthesis of [ 55152-01-7 ]

* 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 [ 55152-01-7 ]

[ 55152-01-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 55152-01-7 ]
  • [ 859154-20-4 ]
YieldReaction ConditionsOperation in experiment
100% With hydrazine In ethanol at 20℃; for 1h; 42 Synthesis 423-(3-Methyl-[1 ,2,4]oxadiazol-5-ylmethyl)-4-oxo-3,4-dihydro-imidazo[5, 1 - d][1 ,2,3,5]tetrazine-8-carboxylic acid amide (CC-003); Hydrazine hydrate (75 μl_, 64% in water) was added to a solution of 3-methyl[1 ,2,4]oxadiazol-5-yl)-acetic acid methyl ester (160 mg, 1.02 mmol) in EtOH (1 mL). The resultant mixture was heated to reflux for 1 hour whereupon it was cooled to room temperature and concentrated in vacuo. Et2O was added to the mixture which was then cooled to 00C. The resulting yellow precipitate was collected by filtration and washed with cold Et2O to give (3-methyl-[1 ,2,4]oxadiazol-5-yl)-acetic acid hydrazide (quantitative yield) in suitably pure form to be used without any further purification.
100% With hydrazine hydrate In ethanol; water for 1h; Reflux;
 

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