2-isobutyrylamino-9-(5'-O-benzoyl-3'-azido-2',3'-dideoxy-β-D-erythro-pentofuranosyl)-6-N-methylallylamino-9H-purine

Base Information

Chemical Name:2-isobutyrylamino-9-(5'-O-benzoyl-3'-azido-2',3'-dideoxy-β-D-erythro-pentofuranosyl)-6-N-methylallylamino-9H-purine
CAS No.:1085745-54-5
Molecular Formula:C₂₅H₂₉N₉O₄
Molecular Weight:519.563
Hs Code.:

Synonyms:2-isobutyrylamino-9-(5'-O-benzoyl-3'-azido-2',3'-dideoxy-β-D-erythro-pentofuranosyl)-6-N-methylallylamino-9H-purine

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Chemical Property of 2-isobutyrylamino-9-(5'-O-benzoyl-3'-azido-2',3'-dideoxy-β-D-erythro-pentofuranosyl)-6-N-methylallylamino-9H-purine

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Technology Process of 2-isobutyrylamino-9-(5'-O-benzoyl-3'-azido-2',3'-dideoxy-β-D-erythro-pentofuranosyl)-6-N-methylallylamino-9H-purine

There total 5 articles about 2-isobutyrylamino-9-(5'-O-benzoyl-3'-azido-2',3'-dideoxy-β-D-erythro-pentofuranosyl)-6-N-methylallylamino-9H-purine 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: 73.0%

: 627-37-2
N-methyl-N-allylamine

: 1085745-47-6
2-isobutyrylamino-9-(5-O-benzoyl-3'-azido-2',3'-dideoxy-β-D-erythro-pentofuranosyl)-6-(2,4,6-triisopropylsulfonyl)-9H-purine

: 1085745-54-5
2-isobutyrylamino-9-(5'-O-benzoyl-3'-azido-2',3'-dideoxy-β-D-erythro-pentofuranosyl)-6-N-methylallylamino-9H-purine

Guidance literature:: In tetrahydrofuran; at 55 ℃; for 15h;

Reference yield:

: 68892-42-2
N-isobutyryl-2'-deoxyguanosine

: 1085745-54-5
2-isobutyrylamino-9-(5'-O-benzoyl-3'-azido-2',3'-dideoxy-β-D-erythro-pentofuranosyl)-6-N-methylallylamino-9H-purine

Guidance literature:: Multi-step reaction with 6 steps

1: dmap; triethylamine / N,N-dimethyl-formamide / 20 °C

2: pyridine; trifluoromethylsulfonic anhydride / dichloromethane / 0.5 h / 0 - 20 °C

3: dmap; triethylamine / dichloromethane / 0.67 h / 0 °C

4: sodium azide / N,N-dimethyl-formamide / 2 h / 120 °C

5: dmap; triethylamine / dichloromethane / 6 - 10 h / 20 °C

6: tetrahydrofuran / 15 h / 55 °C / Heating / reflux

With pyridine; dmap; sodium azide; trifluoromethylsulfonic anhydride; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 104769-15-5
[(2R,3S,5R)-3-hydroxy-5-[2-(2-methylpropanoylamino)-6-oxo-1H-purin-9-yl]tetrahydrofuran-2-yl]methyl benzoate

: 1085745-54-5
2-isobutyrylamino-9-(5'-O-benzoyl-3'-azido-2',3'-dideoxy-β-D-erythro-pentofuranosyl)-6-N-methylallylamino-9H-purine

Guidance literature:: Multi-step reaction with 5 steps

1: pyridine; trifluoromethylsulfonic anhydride / dichloromethane / 0.5 h / 0 - 20 °C

2: dmap; triethylamine / dichloromethane / 0.67 h / 0 °C

3: sodium azide / N,N-dimethyl-formamide / 2 h / 120 °C

4: dmap; triethylamine / dichloromethane / 6 - 10 h / 20 °C

5: tetrahydrofuran / 15 h / 55 °C / Heating / reflux

With pyridine; dmap; sodium azide; trifluoromethylsulfonic anhydride; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;