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[ CAS No. 134790-39-9 ] {[proInfo.proName]}

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Chemical Structure| 134790-39-9
Chemical Structure| 134790-39-9
Structure of 134790-39-9 * Storage: {[proInfo.prStorage]}
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Product Details of [ 134790-39-9 ]

CAS No. :134790-39-9 MDL No. :MFCD09837611
Formula : C23H19F2N3O6 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 471.41 Pubchem ID :-
Synonyms :

Safety of [ 134790-39-9 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501 UN#:N/A
Hazard Statements:H302-H312-H315-H319-H332-H335 Packing Group:N/A
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Application In Synthesis of [ 134790-39-9 ]

* 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 [ 134790-39-9 ]

[ 134790-39-9 ] Synthesis Path-Downstream   1~5

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  • [ 18037-10-0 ]
  • [ 134790-40-2 ]
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  • 2
  • [ 1173824-58-2 ]
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YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 100 percent / triethylamine / CH2Cl2 / 2 h / 23 °C 2: 1) Me3SiOTf / 1) 1,1,2-trichloroethane, r.t., 30 min, 2) 113 deg C, 18 h
Multi-step reaction with 2 steps 1: triethylamine / dichloromethane / 2 h / 5 - 20 °C 2: 3 h / 120 °C / Heating
  • 3
  • [ 122111-01-7 ]
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  • 4
  • [ 134790-39-9 ]
  • [ 95058-81-4 ]
YieldReaction ConditionsOperation in experiment
82.7% With ammonium hydroxide; In methanol; at 20℃; for 3h; Under stirring at room temperature, the compound 4 (330.0g, 0.70 mol) was dissolved in 700.0 ml methanol. Add dropwise concentrated aqueous ammonia (100.0 ml, 28%, 15.0 mol/L). Stir the reaction for more than 3h. After the reaction, water 700.0 ml, decompression of the concentrated solution to the original volume of the 1/2 can be to remove methanol, adding ethyl acetate 500.0 ml, fully stirring 30min. Layered, separating the organic layer. The aqueous layer then adding ethyl acetate 200.0 ml extraction, separating the organic layer, the combined organic layer, adding activated carbon to decolorize, filtering. The filtrate is concentrated under reduced pressure, the residual solid obtained. The residual solid 200.0 ml isopropanol stirring and dissolving, slowly concentrated hydrochloric acid to adjust the pH to 3.5 - 3.7, temperature control in the 70 - 75 C stirring 30min, cooling to room temperature, stirring crystallization 3h above. Filtering to obtain white solid, vacuum oven drying, maintained at a temperature of 45 - 50 C, maintained in the vacuum degree of the 0.08 - 0.1 mpa, drying 6h above, obtain 153.8 g white solid, is compound 5, yield 82.7%.
With sodium t-butanolate; In methanol; at 20℃; for 2h; 2'-deoxy-2 ', 2'-difluoro-cytidine-3', 5'-benzoate (75.0g, 0.16mol, alpha-isomer content of 0.08%),Sodium tert-butoxide (33.6 g, 0.34 mol),Methanol (800ml) in 2L three-necked flask and mix well,Reaction at room temperature 2h,TLC detection reaction was completed,1M hydrochloric acid to adjust the pH to 7,Concentrate to dryness under reduced pressure,Water (1 L),Extraction with ethyl acetate impurity,After the ethyl acetate layer was backwash with a small amount of water,Merged water layer,Activated carbon bleaching,filter,Filtrate spin dry,Isopropyl alcohol (1 L) and concentrated hydrochloric acid (40 ml) were added to the residue,Heated to 70 C,After 30min incubation at room temperature overnight.filter,The filter cake was washed successively with cold isopropanol and n-hexane,dry,Gemcitabine hydrochloride 44.8g,Purity 99.5%alpha isomer content of 0.02%Yield 93.4%.
  • 5
  • [ 134877-42-2 ]
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