9-[(3S,4S,5S)-5-[(benzoyloxy)methyl]-4-(benzyloxy)tetrahydrofuran-3-yl]-6-chloropurine

Base Information

Chemical Name:9-[(3S,4S,5S)-5-[(benzoyloxy)methyl]-4-(benzyloxy)tetrahydrofuran-3-yl]-6-chloropurine
CAS No.:373647-06-4
Molecular Formula:C₂₄H₂₁ClN₄O₄
Molecular Weight:464.908
Hs Code.:

Synonyms:9-[(3S,4S,5S)-5-[(benzoyloxy)methyl]-4-(benzyloxy)tetrahydrofuran-3-yl]-6-chloropurine

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Chemical Property of 9-[(3S,4S,5S)-5-[(benzoyloxy)methyl]-4-(benzyloxy)tetrahydrofuran-3-yl]-6-chloropurine

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Technology Process of 9-[(3S,4S,5S)-5-[(benzoyloxy)methyl]-4-(benzyloxy)tetrahydrofuran-3-yl]-6-chloropurine

There total 6 articles about 9-[(3S,4S,5S)-5-[(benzoyloxy)methyl]-4-(benzyloxy)tetrahydrofuran-3-yl]-6-chloropurine 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:

: 98-88-4
benzoyl chloride

: 373647-06-4
9-[(3S,4S,5S)-5-[(benzoyloxy)methyl]-4-(benzyloxy)tetrahydrofuran-3-yl]-6-chloropurine

Guidance literature:: Multi-step reaction with 5 steps

1.1: 74 percent / pyridine / 1.5 h / -20 °C

2.1: 98 percent / pyridine / 72 h / 4 °C

3.1: 84 percent / NaN₃; 15-crown-5 / dimethylsulfoxide / 100 °C

4.1: Ph₃P / tetrahydrofuran / 2.5 h / 20 °C

4.2: 96 percent / H₂O / tetrahydrofuran / 1 h / Heating

5.1: Et₃N / butan-1-ol / 72 h / Heating

5.2: 42 percent / HCl / H₂O / 72 h

With pyridine; sodium azide; 15-crown-5; triethylamine; triphenylphosphine; In tetrahydrofuran; dimethyl sulfoxide; butan-1-ol;
DOI:10.1016/S0957-4166(01)00283-X

Reference yield:

: 334784-75-7
(2R,3S,4R)-3-benzyloxy-2-(iodomethyl)tetrahydrofuran-4-ol

: 373647-06-4
9-[(3S,4S,5S)-5-[(benzoyloxy)methyl]-4-(benzyloxy)tetrahydrofuran-3-yl]-6-chloropurine

Guidance literature:: Multi-step reaction with 6 steps

1.1: 89 percent / KO₂; 18-crown-6 / dimethylsulfoxide / 0.08 h / 20 °C

2.1: 74 percent / pyridine / 1.5 h / -20 °C

3.1: 98 percent / pyridine / 72 h / 4 °C

4.1: 84 percent / NaN₃; 15-crown-5 / dimethylsulfoxide / 100 °C

5.1: Ph₃P / tetrahydrofuran / 2.5 h / 20 °C

5.2: 96 percent / H₂O / tetrahydrofuran / 1 h / Heating

6.1: Et₃N / butan-1-ol / 72 h / Heating

6.2: 42 percent / HCl / H₂O / 72 h

With pyridine; sodium azide; 15-crown-5; 18-crown-6 ether; triethylamine; triphenylphosphine; In tetrahydrofuran; dimethyl sulfoxide; butan-1-ol;
DOI:10.1016/S0957-4166(01)00283-X

Reference yield:

: 373646-93-6
(3R,4S,5S)-4-(benzyloxy)-5-(hydroxymethyl)tetrahydrofuran-3-ol

: 373647-06-4
9-[(3S,4S,5S)-5-[(benzoyloxy)methyl]-4-(benzyloxy)tetrahydrofuran-3-yl]-6-chloropurine

Guidance literature:: Multi-step reaction with 5 steps

1.1: 74 percent / pyridine / 1.5 h / -20 °C

2.1: 98 percent / pyridine / 72 h / 4 °C

3.1: 84 percent / NaN₃; 15-crown-5 / dimethylsulfoxide / 100 °C

4.1: Ph₃P / tetrahydrofuran / 2.5 h / 20 °C

4.2: 96 percent / H₂O / tetrahydrofuran / 1 h / Heating

5.1: Et₃N / butan-1-ol / 72 h / Heating

5.2: 42 percent / HCl / H₂O / 72 h

With pyridine; sodium azide; 15-crown-5; triethylamine; triphenylphosphine; In tetrahydrofuran; dimethyl sulfoxide; butan-1-ol;
DOI:10.1016/S0957-4166(01)00283-X