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Chemical Structure| 29836-10-0 Chemical Structure| 29836-10-0

Structure of 29836-10-0

Chemical Structure| 29836-10-0

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Product Details of [ 29836-10-0 ]

CAS No. :29836-10-0
Formula : C15H23NO7S
M.W : 361.41
SMILES Code : N[C@H]1[C@@H]([C@@H]([C@@H](CO)O1)O2)OC2(C)C.CC3=CC=C(S(=O)(O)=O)C=C3
MDL No. :MFCD00058116

Safety of [ 29836-10-0 ]

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

Application In Synthesis of [ 29836-10-0 ]

* 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 [ 29836-10-0 ]

[ 29836-10-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4316-94-3 ]
  • [ 29836-10-0 ]
  • [ 116384-42-0 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In N,N-dimethyl-formamide; at 20 - 50℃; for 48.0h; A solution of 2',3'-O-Isopropylidene-beta-D-ribofuranosylamine p-toluenesulfonate salt (1.03 g, 2.85 mmol) in 10 mL of N,N-dimethylformamide at room temperature was treated first with triethylamine (0.662 mL, 4.75 mmol) followed by the slow addition of 6-chloro-5-nitro-pyrimidin-4-ylamine (331 mg, 1.90 mmol). After stirring at 50 C. for 48 h, the solution was diluted with ethyl acetate (30 mL) and washed with water (30 mL). The aqueous phase was further extracted with 20 mL of ethyl acetate and the combined organic extracts were washed with water (30 mL), brine (20 mL), dried over MgSO4, filtered and concentrated in vacuo. The resulting crude product was purified by HPLC to give 6-amino-5-nitro-4-(2',3'-O-isopropylidene-beta-D-ribofuranosylamino)pyrimidine.
With triethylamine; In DMF (N,N-dimethyl-formamide); at 20 - 50℃; for 48.0h; A solution [OF 2', 3'-O-ISOPROPYLIDENE-ss-D-RIBOFURANOSYLAMINE P-TOLUENESULFONATE] salt (1.03 g, 2.85 mmol) in 10 mL of N,N-dimethylformamide at room temperature was treated first with triethylamine (0.662 mL, 4.75 mmol) followed by the slow addition of 6- [CHLORO-5-NITRO-PYRIMIDIN-4-YLAMINE] (331 mg, 1.90 mmol). After stirring at [50C] for 48 h, the solution was diluted with ethyl acetate (30 mL) and washed with water (30 mL). The aqueous phase was further extracted with 20 mL of ethyl acetate and the combined organic extracts were washed with water (30 mL), brine (20 mL), dried over [MGS04,] filtered and concentrated in vacuo. The resulting crude product was purified by HPLC to give [6-AMINO-] [5-NITRO-4-(2', 3'-O-ISOPROPYLIDENE-ss-D-RIBOFURANOSYLAMINO)-PYRIMIDINE
 

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