N6-benzoyl-N9-(3-O-acetyl-2,5-di-O-benzoyl-α-D-arabinofuranosyl)adenine

Base Information

Chemical Name:N6-benzoyl-N9-(3-O-acetyl-2,5-di-O-benzoyl-α-D-arabinofuranosyl)adenine
CAS No.:303041-32-9
Molecular Formula:C₃₃H₂₇N₅O₈
Molecular Weight:621.606
Hs Code.:

Synonyms:N6-benzoyl-N9-(3-O-acetyl-2,5-di-O-benzoyl-α-D-arabinofuranosyl)adenine

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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 N6-benzoyl-N9-(3-O-acetyl-2,5-di-O-benzoyl-α-D-arabinofuranosyl)adenine

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Technology Process of N6-benzoyl-N9-(3-O-acetyl-2,5-di-O-benzoyl-α-D-arabinofuranosyl)adenine

There total 1 articles about N6-benzoyl-N9-(3-O-acetyl-2,5-di-O-benzoyl-α-D-arabinofuranosyl)adenine 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: 87.0%

: 18055-47-5
N-Benzoyl-N,9-bis(trimethylsilyl)adenin

: 1,3-di-O-acetyl-2,5-O-dibenzoyl-D-arabinofuranose

: 303041-32-9
N6-benzoyl-N9-(3-O-acetyl-2,5-di-O-benzoyl-α-D-arabinofuranosyl)adenine

Guidance literature:: With tin(IV) chloride; In acetonitrile; at 20 ℃;
DOI:10.1021/jo0003652

Reference yield: 88.0%

: 303041-32-9
N6-benzoyl-N9-(3-O-acetyl-2,5-di-O-benzoyl-α-D-arabinofuranosyl)adenine

: 199794-20-2
N9-(3-O-acetyl-2,5-di-O-benzoyl-α-D-arabinofuranosyl)adenine

Guidance literature:: With zinc dibromide; In methanol; chloroform; at 20 ℃; for 12h;
DOI:10.1021/jo0003652

Reference yield:

: 303041-32-9
N6-benzoyl-N9-(3-O-acetyl-2,5-di-O-benzoyl-α-D-arabinofuranosyl)adenine

: N1-(3-O-acetyl-5-O-benzoyl-2-deoxy-α-D-erythro-pentofuranosyl)cytidine

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / ZnBr₂ / methanol; CHCl₃ / 12 h / 20 °C

2: 76 percent / 3,6-dimethyl-9-methylcarbazole; Mg(ClO₄)2 / propan-2-ol; H₂O / Photolysis

With magnesium(II) perchlorate; 3,6,9-trimethyl-9H-carbazole; zinc dibromide; In methanol; chloroform; water; isopropyl alcohol; 1: deacylation / 2: Elimination;
DOI:10.1021/jo0003652