1-(2-amino-6-allylaminopurin-9-yl)-2-C-methyl-β-D-ribofuranose 5'-(O-phenyl-N-(S)-1-(isopropoxycarbonyl)ethyl)thiophosphoramidate

Base Information

Chemical Name:1-(2-amino-6-allylaminopurin-9-yl)-2-C-methyl-β-D-ribofuranose 5'-(O-phenyl-N-(S)-1-(isopropoxycarbonyl)ethyl)thiophosphoramidate
CAS No.:1365634-72-5
Molecular Formula:C₂₆H₃₆N₇O₇PS
Molecular Weight:621.654
Hs Code.:

Synonyms:1-(2-amino-6-allylaminopurin-9-yl)-2-C-methyl-β-D-ribofuranose 5'-(O-phenyl-N-(S)-1-(isopropoxycarbonyl)ethyl)thiophosphoramidate

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Chemical Property of 1-(2-amino-6-allylaminopurin-9-yl)-2-C-methyl-β-D-ribofuranose 5'-(O-phenyl-N-(S)-1-(isopropoxycarbonyl)ethyl)thiophosphoramidate

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Technology Process of 1-(2-amino-6-allylaminopurin-9-yl)-2-C-methyl-β-D-ribofuranose 5'-(O-phenyl-N-(S)-1-(isopropoxycarbonyl)ethyl)thiophosphoramidate

There total 4 articles about 1-(2-amino-6-allylaminopurin-9-yl)-2-C-methyl-β-D-ribofuranose 5'-(O-phenyl-N-(S)-1-(isopropoxycarbonyl)ethyl)thiophosphoramidate 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: 40.8%

: 1365255-67-9
(O-phenyl-N-(S)-1-(isopropoxycarbonyl)eth-1-yl)thiophosphoramidic chloride

: 1365634-71-4
C₁₄H₂₀N₆O₄

: 1365634-72-5
1-(2-amino-6-allylaminopurin-9-yl)-2-C-methyl-β-D-ribofuranose 5'-(O-phenyl-N-(S)-1-(isopropoxycarbonyl)ethyl)thiophosphoramidate

Guidance literature:: With 1-methyl-1H-imidazole; In acetonitrile; at 20 ℃; for 24h;

Reference yield:

: (2S/R,3R,4R,5R)-5-((benzoyloxy)methyl)-3-methyltetrahydrofuran-2,3,4-triyltribenzoate

: 1365634-72-5
1-(2-amino-6-allylaminopurin-9-yl)-2-C-methyl-β-D-ribofuranose 5'-(O-phenyl-N-(S)-1-(isopropoxycarbonyl)ethyl)thiophosphoramidate

Guidance literature:: Multi-step reaction with 3 steps

1.1: trimethylsilyl trifluoromethanesulfonate; 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 18 h / 0 - 70 °C

2.1: tetrahydrofuran / Reflux

2.2: 12 h / 20 °C

3.1: 1-methyl-1H-imidazole / acetonitrile / 24 h / 20 °C

With 1-methyl-1H-imidazole; trimethylsilyl trifluoromethanesulfonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; acetonitrile;

Reference yield:

: 641571-44-0
(2R,3R,4R,5R)-2-(2-amino-6-chloro-9H-purin-9-yl)-5-(benzoyloxymethyl)-3-methyltetrahydrofuran-3,4-diyl dibenzoate

: 1365634-72-5
1-(2-amino-6-allylaminopurin-9-yl)-2-C-methyl-β-D-ribofuranose 5'-(O-phenyl-N-(S)-1-(isopropoxycarbonyl)ethyl)thiophosphoramidate

Guidance literature:: Multi-step reaction with 2 steps

1.1: tetrahydrofuran / Reflux

1.2: 12 h / 20 °C

2.1: 1-methyl-1H-imidazole / acetonitrile / 24 h / 20 °C

With 1-methyl-1H-imidazole; In tetrahydrofuran; acetonitrile;