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Chemical Structure| 1037301-09-9 Chemical Structure| 1037301-09-9

Structure of 1037301-09-9

Chemical Structure| 1037301-09-9

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Product Details of [ 1037301-09-9 ]

CAS No. :1037301-09-9
Formula : C9H17NO3
M.W : 187.24
SMILES Code : O=C([C@@]1(N)COCC1)OCCCC
MDL No. :MFCD24627395

Safety of [ 1037301-09-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 1037301-09-9 ]

* 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 [ 1037301-09-9 ]

[ 1037301-09-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 867130-58-3 ]
  • [ 1037301-09-9 ]
  • [ 1360429-41-9 ]
YieldReaction ConditionsOperation in experiment
90% A solution of <strong>[867130-58-3]6-oxo-1,6-dihydro-pyridazine-4-carboxylic acid</strong> (10.5 g, 74.9 mmol), TBTU (25.3 g, 78.7 mmol), triethylamine (20.9 mL) and 40 mL DMF in 200 mL THF was stirred for 30 minutes at ambient temperature. Then n-butyl(S)-3-amino-tetrahydrofuran-3-carboxylate (14.0 g, 74.9 mmol) was added and the mixture was stirred further overnight. For working up the mixture was evaporated to dryness in vacuo and the residue was stirred with 200 mL ethyl acetate. This solution was washed twice with 5% sodium hydrogen carbonate solution, then dried and evaporated down. The product was thus obtained in a yield of 90% of theory. C14H19N3O5 (309.3) Thin layer chromatograph (silica gel; dichloromethane/ethanol 19:1): Rf=0.16
90% With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; at 20℃; [0373] A solution of <strong>[867130-58-3]6-oxo-1,6-dihydro-pyridazine-4-carboxylic acid</strong> (11.5 g), TBTU (25.3 g), triethylamine (20.9 mL) and 40 mL DMF in 200 mL THF was stirred for 30 minutes at ambient temperature. Then n-butyl (S)-3-amino-tetrahydrofuran-3-carboxylate (14.0 g) was added and the mixture was stirred further overnight. For working up the mixture was evaporated to dryness in vacuo and the residue was stirred with 200 mL of ethyl acetate. This solution was washed twice with 5% sodium hydrogen carbonate solution, then dried and evaporated down. The product was thus obtained in a yield of 90% of theory. [0374] C14H19N3O5 (309.3) [0375] Thin layer chromatogram (silica gel; dichloromethane/ethanol 19:1): Rf=0.16
 

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