1-amino-2,5-anhydro-1-deoxy-N-(6-phenethylamino-9H-purin-2-yl)-D-glucitol

Base Information

Chemical Name:1-amino-2,5-anhydro-1-deoxy-N-(6-phenethylamino-9H-purin-2-yl)-D-glucitol
CAS No.:1292814-85-7
Molecular Formula:C₁₉H₂₄N₆O₄
Molecular Weight:400.437
Hs Code.:

Synonyms:1-amino-2,5-anhydro-1-deoxy-N-(6-phenethylamino-9H-purin-2-yl)-D-glucitol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-amino-2,5-anhydro-1-deoxy-N-(6-phenethylamino-9H-purin-2-yl)-D-glucitol

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Technology Process of 1-amino-2,5-anhydro-1-deoxy-N-(6-phenethylamino-9H-purin-2-yl)-D-glucitol

There total 8 articles about 1-amino-2,5-anhydro-1-deoxy-N-(6-phenethylamino-9H-purin-2-yl)-D-glucitol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%

: 1292814-82-4
1-amino-2,5-anhydro-3,4-di-O-benzyl-1-deoxy-N-(6-phenethylamino-9H-purin-2-yl)-D-glucitol

: 1292814-85-7
1-amino-2,5-anhydro-1-deoxy-N-(6-phenethylamino-9H-purin-2-yl)-D-glucitol

Guidance literature:: With boron trichloride; In dichloromethane; at 0 ℃; for 2h;
DOI:10.1016/j.ejmech.2011.01.048

Reference yield:

: 64-04-0
phenethylamine

: 1292814-85-7
1-amino-2,5-anhydro-1-deoxy-N-(6-phenethylamino-9H-purin-2-yl)-D-glucitol

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / butan-1-ol / 6 h / 80 °C

2: sodium tetrafluoroborate / 1,4-dioxane / 2 h / 130 °C / Microwave irradiation

3: boron trichloride / dichloromethane / 2 h / 0 °C

With sodium tetrafluoroborate; boron trichloride; triethylamine; In 1,4-dioxane; dichloromethane; butan-1-ol;
DOI:10.1016/j.ejmech.2011.01.048

Reference yield:

: 157363-84-3
1,2:5,6-dianhydro-3,4-di-O-benzyl-L-iditol

: 1292814-85-7
1-amino-2,5-anhydro-1-deoxy-N-(6-phenethylamino-9H-purin-2-yl)-D-glucitol

Guidance literature:: Multi-step reaction with 4 steps

1: sodium azide; silica gel / acetonitrile / 48 h

2: hydrogen; palladium / ethyl acetate / 1.5 h / 20 °C

3: sodium tetrafluoroborate / 1,4-dioxane / 2 h / 130 °C / Microwave irradiation

4: boron trichloride / dichloromethane / 2 h / 0 °C

With sodium tetrafluoroborate; sodium azide; hydrogen; silica gel; boron trichloride; palladium; In 1,4-dioxane; dichloromethane; ethyl acetate; acetonitrile;
DOI:10.1016/j.ejmech.2011.01.048