Technology Process of 2',3'-dideoxy-3'-fluoroaristeromycin
There total 12 articles about 2',3'-dideoxy-3'-fluoroaristeromycin which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 48 percent / hydrogen fluoride-pyridine, N-bromosuccinimide / tetrahydrofuran / 1.) O deg C, 30 min, 2.) room temp., 2 h
2: 88 percent / tributyltin hydride, α,α'-azobisisobutyronitrile / benzene / 0.17 h / Heating
3: 100 percent / 2N HCl / 8 h / Heating
4: triethylamine
5: 2.) ammonia-methanol
With
hydrogenchloride; N-Bromosuccinimide; ammonia-methanol; azobisisobutyronitrile; tri-n-butyl-tin hydride; pyridine hydrogenfluoride; triethylamine;
In
tetrahydrofuran; benzene;
DOI:10.1248/cpb.42.183
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 9 percent / triphenylphosphine, iodine, imidazole / toluene / 4 h / Heating
2: 100 percent / tributyltin hydride, α,α'-azobisisobutyronitrile / benzene / 0.33 h / Heating
3: 100 percent / 2N HCl / 8 h / Heating
4: triethylamine
5: 2.) ammonia-methanol
With
1H-imidazole; hydrogenchloride; ammonia-methanol; azobisisobutyronitrile; iodine; tri-n-butyl-tin hydride; triethylamine; triphenylphosphine;
In
toluene; benzene;
DOI:10.1248/cpb.42.183
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 83 percent / dimethylformamide / 2 h / Ambient temperature
2: 37 percent / imidazole / dimethylformamide / 10 h / Ambient temperature
3: 1.) phenylchlorothionocarbonate, 2.) tributyltin hydride, α,α'-azobisisobutyronitrile / 1.) CH2Cl2, room temp., 15 min
4: tetrabutylammonium fluoride
5: 28percent ammonium hydroxide
With
1H-imidazole; ammonium hydroxide; azobisisobutyronitrile; tetrabutyl ammonium fluoride; tri-n-butyl-tin hydride; phenylcarbonochloridothioate;
In
N,N-dimethyl-formamide;
DOI:10.1248/cpb.42.183