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Chemical Structure| 106707-52-2 Chemical Structure| 106707-52-2

Structure of 106707-52-2

Chemical Structure| 106707-52-2

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Product Details of [ 106707-52-2 ]

CAS No. :106707-52-2
Formula : C6H13NO3
M.W : 147.17
SMILES Code : N[C@@H]1[C@@H](O)[C@@H](O)[C@H](CO)C1
MDL No. :MFCD14585219

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Application In Synthesis of [ 106707-52-2 ]

* 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 [ 106707-52-2 ]

[ 106707-52-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4316-94-3 ]
  • [ 106707-52-2 ]
  • (1S,2R,3S,5S)-3-(6-amino-5-nitro-pyrimidin-4-ylamino)-5-hydroxymethyl-cyclopentane-1,2-diol [ No CAS ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In N,N-dimethyl-formamide; at 20℃; To a solution of <strong>[4316-94-3]4-amino-6-chloro-5-nitropyrimidine</strong> (320 mg, 1.83 mmol) in N,N-dimethyl formamide (5 mL) and triethylamine (512 muL, 3.67 mmol) was added (1S,2R,3S,5S-3-Amino-5-hydroxymethyl-cyclopentane-1,2-diol (293 mg, 2.02 mmol). The mixture was stirred at room temperature and monitored by thin layer chromatography until starting material was no longer detected The reaction mixture was diluted with water (20 mL) and extracted with diethyl ether (2*10 mL). The organic extract was washed with saturated aqueous sodium chloride (20 mL), dried over MgSO4, filtered and concentrated in vacuo to give the crude product. The product was recrystallized from hot methanol/water to give a 315 mg of (1S,2R,3S,5S)-3-amino-5-nitro-pyrimidinylamino)-5-hydroxymethyl-cyclopentane-1,2-diol as a yellow solid.
With triethylamine; In DMF (N,N-dimethyl-formamide); at 20℃; To a solution of <strong>[4316-94-3]4-amino-6-chloro-5-nitropyrimidine</strong> (320 mg, 1. 83 mmol) in [N, N-] dimethyl formamide (5 mL) and triethylamine [(512, UL,] 3.67 mmol) was added [(LS,] 2R, 3S, [5S)-3-AMINO-5-HYDROXYMETHYL-CYCLOPENTANE-1,] 2-diol (293mg, 2.02 mmol). The mixture was stirred at room temperature and monitored by thin layer chromatography until starting material was no longer detected. The reaction mixture was diluted with water (20 mL) and extracted with diethyl ether (2 x 10 mL). The organic extract was washed with saturated aqueous sodium chloride (20 mL), dried over [MGS04,] filtered and concentrated in vacuo to give the crude product. The product was recrystallized from hot [METHANOL/WATER] to give a 315 mg of [(LS,] [2R,] 3S, [5S)-3- (6-AMINO-5-NITRO-PYRIMIDIN-4-YLAMINO)-5-] hydroxymethyl-cyclopentane-1, 2-diol as a yellow solid
 

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