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Chemical Structure| 1380327-56-9 Chemical Structure| 1380327-56-9

Structure of 1380327-56-9

Chemical Structure| 1380327-56-9

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Product Details of [ 1380327-56-9 ]

CAS No. :1380327-56-9
Formula : C19H17NO5
M.W : 339.34
SMILES Code : O=C(C1(NC(OCC2C3=CC=CC=C3C4=CC=CC=C24)=O)COC1)O
MDL No. :MFCD27664829

Safety of [ 1380327-56-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 1380327-56-9 ]

* 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 [ 1380327-56-9 ]

[ 1380327-56-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 138650-24-5 ]
  • [ 82911-69-1 ]
  • [ 1380327-56-9 ]
YieldReaction ConditionsOperation in experiment
Intermediate 8; 3-(9H-Fluoren-9-ylmethoxycarbonylamino)-oxetane-3-carboxylic acid A solution of (9H-fluoren-9-yl)methyl 2,5-dioxopyrrolidin-1-yl carbonate (3.2 g, 9.5 mmol) in dioxane (30 ml) was added to a solution of <strong>[138650-24-5]3-amino-oxetane-3-carboxylic acid</strong> (1.17 g, 10 mmol) [CAS 138650-24-5; Synlett 1991, 783-784] and potassium carbonate (2.76 g, 20.0 mmol) in water (30 ml). The light yellow opaque solution was stirred at room temperature for 75 minutes. During that time, a white solid precipitated. The mixture was diluted with water and extracted two times with diethyl ether. The white solid did not dissolve and was kept therefore in the aqueous layer, which was acidified to pH 2 by addition of 1N HCl and extracted three times with EtOAc. The combined EtOAc layers were washed with brine, dried with Na2SO4 and evaporated.The crude title compound was obtained as white solid and was used without further purification.
Intermediate 8 3-(9H-Fluoren-9-ylmethoxycarbonylamino)-oxetane-3-carboxylic acidA solution of (9H-fluoren-9-yl)methyl 2,5-dioxopyrrolidin-l-yl carbonate (3.2 g, 9.5 mmol) in dioxane (30 ml) was added to a solution of <strong>[138650-24-5]3-amino-oxetane-3-carboxylic acid</strong> (1.17 g, 10 mmol) [CAS 138650-24-5; Synlett 1991, 783-784] and potassium carbonate (2.76 g, 20.0 mmol) in water (30 ml). The light yellow opaque solution was stirred at room temperature for 75 minutes. During that time, a white solid precipitated. The mixture was diluted with water and extracted two times with diethyl ether. The white solid did not dissolve and was kept therefore in the aqueous layer, which was acidified to pH 2 by addition of IN HC1 and extracted three times with EtOAc. The combined EtOAc layers were washed with brine, dried with Na2S04 and evaporated.The crude title compound was obtained as white solid and was used without further purification.
With potassium carbonate; In 1,4-dioxane; water; at 20℃; for 1.25h;Inert atmosphere; GammaAlpha1 3-(9H-Fluoren-9-ylmethoxycarbonylamino)-oxetane-3-carboxylic acidA solution of (9H-fluoren-9-yl)methyl 2,5-dioxopyrrolidin-l-yl carbonate (3.2 g, 9.5 mmol) in dioxane (30 ml) was added to a solution of <strong>[138650-24-5]3-amino-oxetane-3-carboxylic acid</strong> (1.17 g, 10 mmol) and potassium carbonate (2.76 g, 20.0 mmol) in water (30 ml). The light yellow opaque solution was stirred at room temperature for 75 minutes. During that time, a white solid precipitated. The mixture was diluted with water and extracted two times with diethyl ether. The white solid did not dissolve and was kept therefore in the aqueous layer, which was acidified to pH 2 by addition of IN HC1 and extracted three times with EtOAc. The combined EtOAc layers were washed with brine, dried with Na2S04 and evaporated. The crude title compound was obtained as white solid and was used without further purification.
With potassium carbonate; In 1,4-dioxane; water; at 20℃; for 1.25h;Inert atmosphere; [A] 3-(9H-Fluoren-9-ylmethoxycarbonylamino)-oxetane-3-carboxylic acid A solution of (9H-fluoren-9-yl)methyl 2,5-dioxopyrrolidin-1-yl carbonate (3.2 g, 9.5 mmol) in dioxane (30 ml) was added to a solution of <strong>[138650-24-5]3-amino-oxetane-3-carboxylic acid</strong> (1.17 g, mmol) and potassium carbonate (2.76 g, 20.0 mmol) in water (30 ml). The light yellow opaque solution was stirred at room temperature for 75 minutes. During that time, a white solid precipitated. The mixture was diluted with water and extracted two times with diethyl ether. The white solid did not dissolve and was kept therefore in the aqueous layer, which was acidified to pH 2 by addition of 1N HCl and extracted three times with EtOAc. The combined EtOAc layers were washed with brine, dried with Na2SO4 and evaporated. The crude title compound was obtained as white solid and was used without further purification.

 

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