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Chemical Structure| 1257237-31-2 Chemical Structure| 1257237-31-2

Structure of 1257237-31-2

Chemical Structure| 1257237-31-2

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Product Details of [ 1257237-31-2 ]

CAS No. :1257237-31-2
Formula : C7H13NO2
M.W : 143.18
SMILES Code : C[C@@H]1COCCN1C(C)=O
MDL No. :MFCD28002109

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Application In Synthesis of [ 1257237-31-2 ]

* 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 [ 1257237-31-2 ]

[ 1257237-31-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 923283-54-9 ]
  • [ 1257237-31-2 ]
  • (R,E)-1-methyl-4-((1-(3-methylmorpholino)ethylene)amino)-1H-pyrazole-5-carboxylic acid methyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
68% Methyl 4-amino-1 -methyl-1 H-pyrazole-5-carboxylate (9 g, 52.21 mmol) and 1 - [(3R)-3-methylmorpholin-4-yl]ethan-1 -one (15 g, 94.28 mmol, 1 .81 eq.) were dissolved in DCE (200 ml_, 2.40 mol) and stirred at 0 C for 0.5 h. To this was added phosphorylchlorid (40 g, 247.95 mmol, 4.75 eq.). The resulting solution was stirred for 16 h at 40 C. The reaction was then quenched by the addition of 20 ml_ of NH4CI. The resulting solution was extracted with ethyl acetate and the organic layers combined and concentrated under vacuum. The residue was purified by column chromatography (Method B). Methyl 1 -methyl-4-[(E)-[1 -[(3R)-3-methylmorpholin-4-yl]ethylidene]amino]-1 H-pyrazole-5-carboxylate was isolated as a yellow solid (11 g, 68%); LC-MS (Method J) Rt: 0.664 min, [MH]+ 281.2.
Under nitrogen atmosphere, dissolve (R)-3-methyl-4-acetylmorpholine (1.85g) in anhydrous DCE (10ml), add phosphorus oxychloride (3.56g) at room temperature and keep stirring at room temperature After reacting for 0.5 hrs, 4-amino-1H-pyrazole-3-carboxylic acid methyl ester (1.0 g) was added, and then the reaction was stirred at 80 C. for 4 hrs. LCMS detects the completion of the reaction. The reaction system is first to spin off most of the phosphorus oxychloride, add DCM (200mL), water (50mL), place in an ice bath, add sodium carbonate slowly under stirring to adjust the pH to 8-9, DCM (200mL*5) After the liquid, it was dried with anhydrous Na2SO4 and concentrated under reduced pressure to obtain 2.4 g of the crude product, namely the intermediate S1, which was directly used for the next step.
 

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