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Chemical Structure| 169253-07-0 Chemical Structure| 169253-07-0

Structure of 169253-07-0

Chemical Structure| 169253-07-0

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Product Details of [ 169253-07-0 ]

CAS No. :169253-07-0
Formula : C9H15NO3
M.W : 185.22
SMILES Code : O=C(O)CC1CN(C(C)=O)CCC1
MDL No. :MFCD14582888

Safety of [ 169253-07-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P330-P362-P403+P233-P501

Application In Synthesis of [ 169253-07-0 ]

* 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 [ 169253-07-0 ]

[ 169253-07-0 ] Synthesis Path-Downstream   1~2

YieldReaction ConditionsOperation in experiment
B. 1-N-ACETYL-3-PIPERIDINYLACETIC ACID STR44 The mixture of compounds from Preparative Example 4A (8.56 grams) are reacted with acetic anhydride (8.56 grams) as described in Preparative Example 3A and the crude mixture of products is diluted in methanol (60 ml) and passed over a bed of BioRad AG50WX4 resin (RSO3 H) and the latter is eluted with methanol. The eluates are evaporated to dryness to give the title compound (Yield: 1.23 grams, MH+
  • 2
  • [ 74494-52-3 ]
  • [ 169253-07-0 ]
YieldReaction ConditionsOperation in experiment
With acetic anhydride; In methanol; B. 1-N-ACETYL-3-PIPERIDINYLACETIC ACID STR52 The mixture of compounds from Preparative Example 10A (8.56 grams) were reacted with acetic anhydride (8.56 grams) as described in Preparative Example 5A and the crude mixture of products was taken up in MeOH (60 ml) and passed over a bed of BioRad AG50WX4 resin (RSO3 H) and the latter was eluted with MeOH. The eluates were evaporated to dryness to give the product compound (Yield: 1.23 grams, MH+
With acetic anhydride; In methanol; B. 1-N-ACETYL-3-PIPERIDINYLACETIC ACID STR62 The mixture of compounds from Preparative Example 6A (8.56 grams) were reacted with acetic anhydride (8.56 grams) as described in Preparative Example 5B and the crude mixture of products was diluted in methanol (60 ml) and passed over a bed of BioRad AG50WX4 resin (RSO3 H) and the latter was eluted with methanol. The eluates were evaporated to dryness to give the title compound (Yield: 1.23 grams, MH+ 186).
With acetic anhydride; In methanol; B. 1-N-ACETYL-3-PIPERIDINYLACETIC ACID STR148 The mixture of compounds from Preparative Example 18A (8.56 grams) were reacted with acetic anhydride (8.56 grams) as described in Preparative Example 13A and the crude mixture of products was taken up in MeOH (60 ml) and passed over a bed of BioRad AG50WX4 resin (RSO3 H) and the latter was eluted with MeOH. The eluates were evaporated to dryness to give the title compound (Yield: 1.23 grams, MH+ 186).
 

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