4-(4-chlorophenyl)-2-(β-D-xylofuranosyloxy)-6-(thien-2-yl)nicotinonitrile

Base Information

Chemical Name:4-(4-chlorophenyl)-2-(β-D-xylofuranosyloxy)-6-(thien-2-yl)nicotinonitrile
CAS No.:1313588-87-2
Molecular Formula:C₂₁H₁₇ClN₂O₅S
Molecular Weight:444.895
Hs Code.:

Synonyms:4-(4-chlorophenyl)-2-(β-D-xylofuranosyloxy)-6-(thien-2-yl)nicotinonitrile

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Chemical Property of 4-(4-chlorophenyl)-2-(β-D-xylofuranosyloxy)-6-(thien-2-yl)nicotinonitrile

Chemical Property:

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Technology Process of 4-(4-chlorophenyl)-2-(β-D-xylofuranosyloxy)-6-(thien-2-yl)nicotinonitrile

There total 5 articles about 4-(4-chlorophenyl)-2-(β-D-xylofuranosyloxy)-6-(thien-2-yl)nicotinonitrile 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: 85.0%

: 1313588-82-7
4-(4-chlorophenyl)-2-(2',3',5'-tri-O-acetyl-β-D-xylofuranosyloxy)-6-(thien-2-yl)nicotinonitrile

: 1313588-87-2
4-(4-chlorophenyl)-2-(β-D-xylofuranosyloxy)-6-(thien-2-yl)nicotinonitrile

Guidance literature:: With water; triethylamine; In methanol; at 20 ℃;
DOI:10.1016/j.ejmech.2011.04.019

Reference yield:

: 88-15-3,97511-16-5
2-Acetylthiophene

: 1313588-87-2
4-(4-chlorophenyl)-2-(β-D-xylofuranosyloxy)-6-(thien-2-yl)nicotinonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydroxide

2.1: ammonium acetate / ethanol / 10 h / Reflux

3.1: potassium carbonate / N,N-dimethyl-formamide; acetone / 1 h

3.2: Reflux

4.1: water; triethylamine / methanol / 20 °C

With ammonium acetate; water; potassium carbonate; triethylamine; sodium hydroxide; In methanol; ethanol; N,N-dimethyl-formamide; acetone;
DOI:10.1016/j.ejmech.2011.04.019

Reference yield:

: 104-88-1
4-chlorobenzaldehyde

: 1313588-87-2
4-(4-chlorophenyl)-2-(β-D-xylofuranosyloxy)-6-(thien-2-yl)nicotinonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydroxide

2.1: ammonium acetate / ethanol / 10 h / Reflux

3.1: potassium carbonate / N,N-dimethyl-formamide; acetone / 1 h

3.2: Reflux

4.1: water; triethylamine / methanol / 20 °C

With ammonium acetate; water; potassium carbonate; triethylamine; sodium hydroxide; In methanol; ethanol; N,N-dimethyl-formamide; acetone;
DOI:10.1016/j.ejmech.2011.04.019