N⁶-benzoyl-5'-O-(2,2,5,5-tetramethylpyrrolidin-3-one-1-sulfinyl)-3'-O-levulinyl-2'-deoxyadenosine

Base Information

• Chemical Name: N⁶-benzoyl-5'-O-(2,2,5,5-tetramethylpyrrolidin-3-one-1-sulfinyl)-3'-O-levulinyl-2'-deoxyadenosine
• CAS No.: 753456-22-3
• Molecular Formula: C₃₀H₃₆N₆O₈S
• Molecular Weight: 640.717

Synonyms:N⁶-benzoyl-5'-O-(2,2,5,5-tetramethylpyrrolidin-3-one-1-sulfinyl)-3'-O-levulinyl-2'-deoxyadenosine

Chemical Property of N⁶-benzoyl-5'-O-(2,2,5,5-tetramethylpyrrolidin-3-one-1-sulfinyl)-3'-O-levulinyl-2'-deoxyadenosine

Chemical Property:

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Technology Process of N⁶-benzoyl-5'-O-(2,2,5,5-tetramethylpyrrolidin-3-one-1-sulfinyl)-3'-O-levulinyl-2'-deoxyadenosine

There total 4 articles about N⁶-benzoyl-5'-O-(2,2,5,5-tetramethylpyrrolidin-3-one-1-sulfinyl)-3'-O-levulinyl-2'-deoxyadenosine 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:

2,2,5,5-tetramethyl-3-pyrroline-3-carboxamide (19805-75-5) → N6-benzoyl-5'-O-(2,2,5,5-tetramethylpyrrolidin-3-one-1-sulfinyl)-3'-O-levulinyl-2'-deoxyadenosine (753456-22-3)

Guidance literature:

Multi-step reaction with 2 steps

1.1: 40 percent / Br; aq. NaOH / 1 h / 100 °C

2.1: triethylamine; thionyl chloride / acetonitrile / 0.17 h / 5 °C

2.2: 78 percent / CH₂Cl₂ / 2 h / 25 °C

With sodium hydroxide; thionyl chloride; bromine; triethylamine; In acetonitrile; 1.1: Hofmann rearrangement;

DOI:10.1021/ja048377i

Reference yield:

5'-O-(4,4'-dimethoxytrityl)-N6-benzoyl-3'-O-levulinoyl-2'-deoxyadenosine (93134-36-2) → N6-benzoyl-5'-O-(2,2,5,5-tetramethylpyrrolidin-3-one-1-sulfinyl)-3'-O-levulinyl-2'-deoxyadenosine (753456-22-3)

Guidance literature:

Multi-step reaction with 2 steps

1.1: acetic acid / 0.5 h / 25 °C

2.1: triethylamine; thionyl chloride / acetonitrile / 0.17 h / 5 °C

2.2: 78 percent / CH₂Cl₂ / 2 h / 25 °C

With thionyl chloride; acetic acid; triethylamine; In acetonitrile;

DOI:10.1021/ja048377i

Reference yield:

levulinic acid (123-76-2) → N6-benzoyl-5'-O-(2,2,5,5-tetramethylpyrrolidin-3-one-1-sulfinyl)-3'-O-levulinyl-2'-deoxyadenosine (753456-22-3)

Guidance literature:

Multi-step reaction with 3 steps

1.1: 1,3-dicyclohexylcarbodiimide; (N,N-dimethylamino)pyridine / dioxane / 3 h / 25 °C

2.1: acetic acid / 0.5 h / 25 °C

3.1: triethylamine; thionyl chloride / acetonitrile / 0.17 h / 5 °C

3.2: 78 percent / CH₂Cl₂ / 2 h / 25 °C

With dmap; thionyl chloride; acetic acid; triethylamine; dicyclohexyl-carbodiimide; In 1,4-dioxane; acetonitrile;

DOI:10.1021/ja048377i

upstream raw materials:

2,2,5,5-tetramethyl-3-pyrroline-3-carboxamide

5'-O-(4,4'-dimethoxytrityl)-N⁶-benzoyl-3'-O-levulinoyl-2'-deoxyadenosine

levulinic acid

N₆-benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-deoxyadenosine

Downstream raw materials:

N⁶-benzoyl-5'-O-(2,2,5,5-tetramethylpyrrolidin-3-one-1-sulfinyl)-3'-O-[(N,N-diisopropylamino)(2-cyanoethyloxy)]phosphinyl-2'-deoxyadenosine

N⁶-benzoyl-5'-O-(2,2,5,5-tetramethylpyrrolidin-3-one-1-sulfinyl)-2'-deoxyadenosine

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