4-amino-6-(3-bromophenyl)-7-(β-L-xylofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carboxamide

Base Information

Chemical Name:4-amino-6-(3-bromophenyl)-7-(β-L-xylofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carboxamide
CAS No.:1350887-41-0
Molecular Formula:C₁₈H₁₈BrN₅O₅
Molecular Weight:464.275
Hs Code.:

Synonyms:4-amino-6-(3-bromophenyl)-7-(β-L-xylofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carboxamide

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Chemical Property of 4-amino-6-(3-bromophenyl)-7-(β-L-xylofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carboxamide

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Technology Process of 4-amino-6-(3-bromophenyl)-7-(β-L-xylofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carboxamide

There total 11 articles about 4-amino-6-(3-bromophenyl)-7-(β-L-xylofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carboxamide 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: 84.0%

: 1350887-34-1
4-amino-6-(3-bromophenyl)-5-cyano-7-(β-L-xylofuranosyl)pyrrolo[2,3-d]pyrimidine

: 1350887-41-0
4-amino-6-(3-bromophenyl)-7-(β-L-xylofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carboxamide

Guidance literature:: With ammonium hydroxide; dihydrogen peroxide; In methanol; at 20 ℃;
DOI:10.1016/j.bmc.2011.10.003

Reference yield:

: 1350887-25-0
4-amino-6-(3-bromophenyl)-5-cyano-7-(2,3,5-tri-O-benzoyl-β-L-xylofuranosyl)pyrrolo[2,3-d]pyrimidine

: 1350887-41-0
4-amino-6-(3-bromophenyl)-7-(β-L-xylofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium methylate / methanol / 12 h / 20 °C

2: ammonium hydroxide; dihydrogen peroxide / methanol / 20 °C

With ammonium hydroxide; dihydrogen peroxide; sodium methylate; In methanol;
DOI:10.1016/j.bmc.2011.10.003

Reference yield:

: 3080-30-6,6974-32-9,14215-97-5,16162-35-9,20822-87-1,21138-42-1,22249-15-6,22249-17-8,26287-72-9,53403-35-3,53403-36-4,57236-69-8,70832-64-3,99395-04-7,100101-51-7,109668-83-9,120019-54-7
1-O-acetyl-2,3,5-tri-O-benzoyl-β-L-ribofuranose

: 1350887-41-0
4-amino-6-(3-bromophenyl)-7-(β-L-xylofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: N,O-bis-(trimethylsilyl)-acetamide / acetonitrile / 0.5 h / 20 °C / Inert atmosphere

1.2: 3.17 h / 20 - 80 °C

2.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate / toluene / 24 h / Inert atmosphere; Reflux

3.1: sodium methylate / methanol / 12 h / 20 °C

4.1: ammonium hydroxide; dihydrogen peroxide / methanol / 20 °C

With ammonium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; N,O-bis-(trimethylsilyl)-acetamide; dihydrogen peroxide; sodium methylate; potassium carbonate; In methanol; toluene; acetonitrile; 2.1: Suzuki coupling;
DOI:10.1016/j.bmc.2011.10.003