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inquiryUnique advantages for 2-Deoxy-2-Fluoro-1,3,5-tri-O-Benzoyl-D-ribofuranose Cas 97614-43-2 Guaranteed the purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:White powder Storage:Normal te
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inquiryName: 2-Deoxy-2-fluoro-1,3,5-tri-O-benzoyl-D-ribofuranose CAS:97614-43-2 MF: C26H21FO7 Appearance:White crystal Storage:Store in cool and dry place, away from sun light. Package:25kg Application:Anticancer drug intermediates Transportation:By se
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inquiryBest quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
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inquiryWhy Choose Us: 1. Factory direct sales, so we can provide the competitive price and high quality product base on 8 years of production and R&D experience. 2. It is available in stock for quick shipment.Products could be packaged according to cu
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inquiry2-O-<(trifluoromethyl)sulfonyl>-1,3,5-tri-O-benzoyl-α-D-ribofuranose
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
Conditions | Yield |
---|---|
With triethylamine tris(hydrogen fluoride) In ethyl acetate at 80℃; for 24h; Substitution; | 85% |
With triethylamine tris(hydrogen fluoride); triethylamine In acetonitrile at 50℃; for 18h; | |
With hydrogen fluoride; tetrabutylammonium bicarbonate In acetonitrile at 80℃; for 0.5h; |
1,3,5-tri-O-benzoyl-α-D-ribofuranoside
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
Conditions | Yield |
---|---|
With (bis-(2-methoxyethyl)amino)sulfur trufluoride In dichloromethane at 50℃; | 83% |
With diethylamino-sulfur trifluoride In dichloromethane at 40℃; | 75% |
Multi-step reaction with 2 steps 1: pyridine / acetonitrile / 0.5 h / 20 °C 2: Et3N(HF)3; Et3N / acetonitrile / 18 h / 50 °C View Scheme | |
Multi-step reaction with 2 steps 1: 100 percent / CH2Cl2; pyridine / -10 °C 2: 85 percent / Et3N*3HF / ethyl acetate / 24 h / 80 °C View Scheme | |
With diethylamino-sulfur trifluoride |
2-O-(imidazolylsulfonyl)-1,3,5-tri-O-benzoyl-α-D-ribofuranose
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
Conditions | Yield |
---|---|
With triethylamine tris(hydrogen fluoride) In ethyl acetate at 60 - 70℃; for 4.5h; | 66.4% |
Multi-step reaction with 2 steps 1: 77 percent / Et3N*HF / ethyl acetate 2: (But)4NF / ethyl acetate / 0.33 h / 70 °C View Scheme | |
Multi-step reaction with 2 steps 1: Et3N*3HF / ethyl acetate / 20 - 60 °C 2: Et3N*3HF / ethyl acetate / 70 °C View Scheme |
2-O-(imidazolylsulfonyl)-1,3,5-tri-O-benzoyl-α-D-ribofuranose
A
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
B
2-O-(fluorosulfonyl)-1,3,5-tri-O-benzoyl-α-D-ribofuranose
Conditions | Yield |
---|---|
With potassium hydrogen bifluoride; hydrogen fluoride In various solvent(s) at 160℃; for 1h; | A 62.8% B n/a |
2-O-(fluorosulfonyl)-1,3,5-tri-O-benzoyl-α-D-ribofuranose
A
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
Conditions | Yield |
---|---|
With hydrogen fluoride; triethylamine In ethyl acetate at 71 - 72℃; for 4h; Product distribution; Further Variations:; Reagents; Solvents; reaction time; Substitution; | A 60.5% B n/a |
2-O-<(trifluoromethyl)sulfonyl>-1,3,5-tri-O-benzoyl-α-D-ribofuranose
A
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In ethyl acetate at 71 - 72℃; for 0.333333h; Substitution; | A 34% B n/a |
ethylene glycol
2-O-(imidazolylsulfonyl)-1,3,5-tri-O-benzoyl-α-D-ribofuranose
A
β-phenyl hydroxypropionate
B
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
C
C28H26O9
Conditions | Yield |
---|---|
With potassium hydrogen bifluoride; hydrogen fluoride In various solvent(s) at 160℃; for 1h; Product distribution; other reaction conditions; |
2-O-(fluorosulfonyl)-1,3,5-tri-O-benzoyl-α-D-ribofuranose
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
Conditions | Yield |
---|---|
With triethylamine tris(hydrogen fluoride) In ethyl acetate at 70℃; Yield given; | |
With tetrabutyl ammonium fluoride In ethyl acetate at 70℃; for 0.333333h; Substitution; |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
2-deoxy-2-fluoro-3,5-di-O-benzoyl-α-D-arabinofuranosyl bromide
Conditions | Yield |
---|---|
With hydrogen bromide; acetic acid In dichloromethane at -5 - 20℃; for 18.33h; Inert atmosphere; | 100% |
With hydrogen bromide; acetic acid In dichloromethane for 20h; Ambient temperature; | 99% |
With hydrogen bromide; acetic acid In dichloromethane at 20℃; | 99% |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
((2R,3R,4S)-3-(benzoyloxy)-5-bromo-4-fluorotetrahydrofuran-2-yl)methyl benzoate
Conditions | Yield |
---|---|
With hydrogen bromide; acetic acid | 99% |
With hydrogen bromide; acetic acid In dichloromethane at 20℃; | 99% |
With acetic acid |
dichloromethane
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
((2R,3R,4S)-3-(benzoyloxy)-5-bromo-4-fluorotetrahydrofuran-2-yl)methyl benzoate
Conditions | Yield |
---|---|
With hydrogen bromide; acetic acid | 90% |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
sevoflurane
Conditions | Yield |
---|---|
With potassium fluoride In various solvent(s) at 95℃; for 1h; Substitution; | 71% |
octanol
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
B
octyl 2-deoxy-2-fluoro-3,5-di-O-benzoyl-α-D-arabinofuranoside
Conditions | Yield |
---|---|
Stage #1: 1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose With tin(IV) chloride In acetonitrile at 20℃; for 0.25h; Molecular sieve; Inert atmosphere; Stage #2: octanol In acetonitrile at 20℃; for 1.5h; Inert atmosphere; Stage #3: With triethylamine In dichloromethane | A n/a B 54% |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
9-Trimethylsilyl-2,6-dichlorpurin
C
((2R,3R,4S,5R)-3-(benzoyloxy)-5-(2,6-dichloro-9H-purin-9-yl)-4-fluorotetrahydrofuran-2-yl)methyl benzoate
D
C24H17Cl2FN4O5
Conditions | Yield |
---|---|
With trimethylsilyl trifluoromethanesulfonate In acetonitrile for 0.333333h; Heating; | A 5% B n/a C 35% D 33% |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
6-benzoylamino-9-trimethylsilylpurine
A
9-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)adenine
B
9-(2-deoxy-2-fluoro-α-D-arabinofuranosyl)adenine
Conditions | Yield |
---|---|
Stage #1: 1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose; 6-benzoylamino-9-trimethylsilylpurine With trimethylsilyl trifluoromethanesulfonate In acetonitrile for 4h; Heating; Stage #2: With ammonia In methanol at 20℃; for 48h; | A 14% B 14% C 25% |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
2,4-bis(trimethylsiloxy)-5-methylpyrimidine
Conditions | Yield |
---|---|
With tin(IV) chloride In acetonitrile at 80 - 81℃; for 0.75h; |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
4-amino-7-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-5-fluoro-7H-pyrrolo[2,3-d]pyrimidine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: HBr; AcOH / CH2Cl2 / 16 h / 20 °C 2.1: KOH; tris[2-(2-methoxyethoxy)ethyl]amine / acetonitrile / 0.25 h / 20 °C 2.2: 61.7 percent / acetonitrile / 0.17 h / 20 °C 3.1: 72 percent / aq. NH3 / dioxane / 16 h / 120 °C View Scheme |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
7-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-5-fluoro-4-methoxy-7H-pyrrolo[2,3-d]pyrimidine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: HBr; AcOH / CH2Cl2 / 16 h / 20 °C 2.1: KOH; tris[2-(2-methoxyethoxy)ethyl]amine / acetonitrile / 0.25 h / 20 °C 2.2: 61.7 percent / acetonitrile / 0.17 h / 20 °C 3.1: 97 percent / NaOMe / 12 h / 20 °C View Scheme |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: HBr; AcOH / CH2Cl2 / 16 h / 20 °C 2.1: KOH; tris[2-(2-methoxyethoxy)ethyl]amine / acetonitrile / 0.25 h / 20 °C 2.2: 61.7 percent / acetonitrile / 0.17 h / 20 °C 3.1: 97 percent / NaOMe / 12 h / 20 °C 4.1: 37 percent / aq. NaOH / 1 h / Heating View Scheme |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
4-chloro-7-(2-deoxy-3,5-di-O-benzoyl-β-D-arabinofuranosyl)-5-fluoro-7H-pyrrolo[2,3-d]pyrimidine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: HBr; AcOH / CH2Cl2 / 16 h / 20 °C 2.1: KOH; tris[2-(2-methoxyethoxy)ethyl]amine / acetonitrile / 0.25 h / 20 °C 2.2: 61.7 percent / acetonitrile / 0.17 h / 20 °C View Scheme | |
Multi-step reaction with 2 steps 1.1: hydrogen bromide; acetic acid 2.1: Tris(3,6-dioxaheptyl)amine; potassium hydroxide / acetonitrile / 0.25 h / 20 °C 2.2: 0.17 h / 20 °C View Scheme |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: HBr; acetic acid / 1,2-dichloro-ethane / 0.17 h / 80 °C 2: 1,2-dichloro-ethane / 1 h / 110 °C 3: sodium methoxide / methanol / 0.17 h / 80 °C View Scheme |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: HBr; acetic acid / 1,2-dichloro-ethane / 0.17 h / 80 °C 2: 1,2-dichloro-ethane / 1 h / 110 °C 3: sodium methoxide / methanol / 0.17 h / 80 °C View Scheme |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: HBr; acetic acid / 1,2-dichloro-ethane / 0.17 h / 80 °C 2: 1,2-dichloro-ethane / 1 h / 110 °C 3: sodium methoxide / methanol / 0.17 h / 80 °C View Scheme |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: HBr; acetic acid / 1,2-dichloro-ethane / 0.17 h / 80 °C 2: 1,2-dichloro-ethane / 1 h / 110 °C 3: sodium methoxide / methanol / 0.17 h / 80 °C View Scheme |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: HBr; acetic acid / 1,2-dichloro-ethane / 0.17 h / 80 °C 2: 1,2-dichloro-ethane / 1 h / 110 °C View Scheme |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: HBr; acetic acid / 1,2-dichloro-ethane / 0.17 h / 80 °C 2: 1,2-dichloro-ethane / 1 h / 110 °C View Scheme |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: HBr; acetic acid / 1,2-dichloro-ethane / 0.17 h / 80 °C 2: 1,2-dichloro-ethane / 1 h / 110 °C View Scheme |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-5-propyluracil
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: HBr; acetic acid / 1,2-dichloro-ethane / 0.17 h / 80 °C 2: 1,2-dichloro-ethane / 1 h / 110 °C 3: sodium methoxide / methanol / 0.17 h / 80 °C View Scheme |
1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-D-arabinofuranose
1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-5-(trifluromethyl)uracil
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: HBr; acetic acid / 1,2-dichloro-ethane / 0.17 h / 80 °C 2: 1,2-dichloro-ethane / 1 h / 110 °C 3: sodium methoxide / methanol / 0.17 h / 80 °C View Scheme |
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