Technology Process of (2R,3S,5R)-5-(4-Chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-2-(hydroxymethyl)tetrahydrofuran-3-ol
There total 1 articles about (2R,3S,5R)-5-(4-Chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-2-(hydroxymethyl)tetrahydrofuran-3-ol which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine;
With
potassium hydroxide; Tris(3,6-dioxaheptyl)amine;
In
acetonitrile;
at 20 ℃;
for 0.166667h;
2-deoxy-3,5-di-O-p-toluoyl-α-D-erythro-pentofuranosyl chloride;
In
acetonitrile;
at 20 ℃;
for 1h;
With
ammonia;
In
methanol;
at 20 ℃;
for 24h;
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 1H-imidazole / N,N-dimethyl-formamide / 16 h / 20 °C
2: bis(benzonitrile)palladium(II) dichloride; triethylamine / 1,4-dioxane / 48 h / 50 °C
3: lithium borohydride / tetrahydrofuran; methanol / 0.92 h / 20 °C / Reflux
4: tetrabutylammomium bromide; sodium hydroxide / dichloromethane / 48 h / 20 °C / Darkness
With
1H-imidazole; bis(benzonitrile)palladium(II) dichloride; lithium borohydride; tetrabutylammomium bromide; triethylamine; sodium hydroxide;
In
tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/anie.201106516
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 1H-imidazole / N,N-dimethyl-formamide / 16 h / 20 °C
2: bis(benzonitrile)palladium(II) dichloride; triethylamine / 1,4-dioxane / 48 h / 50 °C
3: lithium borohydride / tetrahydrofuran; methanol / 0.92 h / 20 °C / Reflux
4: tetrabutylammomium bromide; sodium hydroxide / dichloromethane / 48 h / 20 °C / Darkness
5: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 0 - 20 °C
6: ammonia / 1,4-dioxane; methanol / 16 h / 100 °C
With
1H-imidazole; bis(benzonitrile)palladium(II) dichloride; lithium borohydride; tetrabutyl ammonium fluoride; tetrabutylammomium bromide; ammonia; triethylamine; sodium hydroxide;
In
tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/anie.201106516