(Z)-6-(6-aminopyridin-3-yl)-2-benzylidenebenzofuran-3(2H)-one

Base Information

• Chemical Name: (Z)-6-(6-aminopyridin-3-yl)-2-benzylidenebenzofuran-3(2H)-one
• CAS No.: 1613190-12-7
• Molecular Formula: C₂₀H₁₄N₂O₂
• Molecular Weight: 314.343
• Mol file: 1613190-12-7.mol

Synonyms:(Z)-6-(6-aminopyridin-3-yl)-2-benzylidenebenzofuran-3(2H)-one

Chemical Property of (Z)-6-(6-aminopyridin-3-yl)-2-benzylidenebenzofuran-3(2H)-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (Z)-6-(6-aminopyridin-3-yl)-2-benzylidenebenzofuran-3(2H)-one

There total 4 articles about (Z)-6-(6-aminopyridin-3-yl)-2-benzylidenebenzofuran-3(2H)-one 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: 98.0%

2-amino-5-pyridinyl boronic acid (851524-96-4) + (Z)-2-benzylidene-3-oxo-2,3-dihydrobenzofuran-6-yl trifluoromethanesulfonate (1613190-18-3) → (Z)-6-(6-aminopyridin-3-yl)-2-benzylidenebenzofuran-3(2H)-one (1613190-12-7)

Guidance literature:

With bis-triphenylphosphine-palladium(II) chloride; sodium carbonate; In 1,4-dioxane; at 100 ℃; for 3h; Inert atmosphere;

DOI:10.1016/j.ejmech.2014.04.076

Reference yield:

6-hydroxybenzofuran-3-one (6272-26-0) → (Z)-6-(6-aminopyridin-3-yl)-2-benzylidenebenzofuran-3(2H)-one (1613190-12-7)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium hydroxide / water / 4 h / 20 °C

2: triethylamine / dichloromethane / 0.75 h / 20 °C / Inert atmosphere

3: bis-triphenylphosphine-palladium(II) chloride; sodium carbonate / 1,4-dioxane / 3 h / 100 °C / Inert atmosphere

With bis-triphenylphosphine-palladium(II) chloride; sodium carbonate; triethylamine; potassium hydroxide; In 1,4-dioxane; dichloromethane; water; 3: |Suzuki-Miyaura Coupling;

DOI:10.1016/j.ejmech.2014.04.076

Reference yield:

benzaldehyde (100-52-7) → (Z)-6-(6-aminopyridin-3-yl)-2-benzylidenebenzofuran-3(2H)-one (1613190-12-7)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium hydroxide / water / 4 h / 20 °C

2: triethylamine / dichloromethane / 0.75 h / 20 °C / Inert atmosphere

3: bis-triphenylphosphine-palladium(II) chloride; sodium carbonate / 1,4-dioxane / 3 h / 100 °C / Inert atmosphere

With bis-triphenylphosphine-palladium(II) chloride; sodium carbonate; triethylamine; potassium hydroxide; In 1,4-dioxane; dichloromethane; water; 3: |Suzuki-Miyaura Coupling;

DOI:10.1016/j.ejmech.2014.04.076

upstream raw materials:

2-amino-5-pyridinyl boronic acid

(Z)-2-benzylidene-3-oxo-2,3-dihydrobenzofuran-6-yl trifluoromethanesulfonate

benzaldehyde

6-hydroxybenzofuran-3-one