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Chemical Structure| 1007358-76-0 Chemical Structure| 1007358-76-0

Structure of 1007358-76-0

Chemical Structure| 1007358-76-0

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Product Details of [ 1007358-76-0 ]

CAS No. :1007358-76-0
Formula : C22H22N2O4
M.W : 378.42
SMILES Code : C([C@@H](OC=1N=C(C)C=C(C)N1)C(O)=O)(OC)(C2=CC=CC=C2)C3=CC=CC=C3
MDL No. :N/A

Safety of [ 1007358-76-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H303-H361
Precautionary Statements:P501-P202-P201-P280-P312-P405

Application In Synthesis of [ 1007358-76-0 ]

* 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 [ 1007358-76-0 ]

[ 1007358-76-0 ] Synthesis Path-Downstream   1~2

  • 1
  • (S)-1-(2,4-dichlorophenyl)ethylammonium (S)-2-hydroxy-3-methoxy-3,3-diphenylpropionate [ No CAS ]
  • [ 35144-22-0 ]
  • [ 1007358-76-0 ]
YieldReaction ConditionsOperation in experiment
77.14% Similarly, (R)-Ambrisentan was prepared in different batch and the results are summarized in Table 5 given below.Table 5:
  • 2
  • [ 1260633-84-8 ]
  • [ 35144-22-0 ]
  • [ 1007358-76-0 ]
YieldReaction ConditionsOperation in experiment
77.14% With lithium hydride; In N,N-dimethyl-formamide; at 30 - 32℃; for 48h; In a 25 mL three necked flask, (0.150 g) (S) 2,4-dichlorophenethyl ammonium salt of (S) 2-hydroxy-3-methoxy 3,3-diphenyl propionate, 22.68 mg lithium hydride and 3 mL DMF were taken. Subsequently, (76 mg) 4,6-dimethyl-2-methylsulfonyl pyrimidine was added in to the reaction mixture. Reaction mixture was stirred at 30-32 C. for 48 hours and diluted with water. After suitable work up and acidification gives 94.7 mg (R)-Ambrisentan
 

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