(1-benzyl-1H-indol-3-yl)-(4-hydroxy-6-methoxy-2-methyl-pyridin-3-yl)-methanone

Base Information

• Chemical Name: (1-benzyl-1H-indol-3-yl)-(4-hydroxy-6-methoxy-2-methyl-pyridin-3-yl)-methanone
• CAS No.: 797050-70-5
• Molecular Formula: C₂₃H₂₀N₂O₃
• Molecular Weight: 372.423
• Mol file: 797050-70-5.mol

Synonyms:(1-benzyl-1H-indol-3-yl)-(4-hydroxy-6-methoxy-2-methyl-pyridin-3-yl)-methanone

Chemical Property of (1-benzyl-1H-indol-3-yl)-(4-hydroxy-6-methoxy-2-methyl-pyridin-3-yl)-methanone

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (1-benzyl-1H-indol-3-yl)-(4-hydroxy-6-methoxy-2-methyl-pyridin-3-yl)-methanone

There total 6 articles about (1-benzyl-1H-indol-3-yl)-(4-hydroxy-6-methoxy-2-methyl-pyridin-3-yl)-methanone 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: 99.0%

(1-benzyl-1H-indol-3-yl)-(4,6-dimethoxy-2-methyl-pyridin-3-yl)-methanone (797050-69-2) → (1-benzyl-1H-indol-3-yl)-(4-hydroxy-6-methoxy-2-methyl-pyridin-3-yl)-methanone (797050-70-5)

Guidance literature:

With boron tribromide; In dichloromethane;

DOI:10.1055/s-2004-831317

Reference yield:

2,4,6-trimethoxypyridine (91591-88-7) → (1-benzyl-1H-indol-3-yl)-(4-hydroxy-6-methoxy-2-methyl-pyridin-3-yl)-methanone (797050-70-5)

Guidance literature:

Multi-step reaction with 6 steps

1: 97 percent / TiCl₄ / CH₂Cl₂ / 18 h / 20 °C

2: 94 percent / 2CuO*Cr₂O₃ / quinoline / 180 °C

3: 94 percent / HBr; AcOH / 50 °C

4: 94 percent / Et₃N / CH₂Cl₂

5: 79 percent / NiCl₂(dppe)2

6: 99 percent / BBr₃ / CH₂Cl₂

With chromium(III) oxide; hydrogen bromide; boron tribromide; titanium tetrachloride; acetic acid; triethylamine; copper(II) oxide; Ni(DPPE)2Cl₂; In quinoline; dichloromethane; 1: Friedel-Crafts reaction;

DOI:10.1055/s-2004-831317

Reference yield:

1-benzylindole-2,3-dicarboxylic anhydride (151054-77-2) → (1-benzyl-1H-indol-3-yl)-(4-hydroxy-6-methoxy-2-methyl-pyridin-3-yl)-methanone (797050-70-5)

Guidance literature:

Multi-step reaction with 6 steps

1: 97 percent / TiCl₄ / CH₂Cl₂ / 18 h / 20 °C

2: 94 percent / 2CuO*Cr₂O₃ / quinoline / 180 °C

3: 94 percent / HBr; AcOH / 50 °C

4: 94 percent / Et₃N / CH₂Cl₂

5: 79 percent / NiCl₂(dppe)2

6: 99 percent / BBr₃ / CH₂Cl₂

With chromium(III) oxide; hydrogen bromide; boron tribromide; titanium tetrachloride; acetic acid; triethylamine; copper(II) oxide; Ni(DPPE)2Cl₂; In quinoline; dichloromethane; 1: Friedel-Crafts reaction;

DOI:10.1055/s-2004-831317

upstream raw materials:

(1-benzyl-1H-indol-3-yl)-(4,6-dimethoxy-2-methyl-pyridin-3-yl)-methanone

2,4,6-trimethoxypyridine

1-benzylindole-2,3-dicarboxylic anhydride

1-benzyl-3-(2-hydroxy-4,6-dimethoxynicotinoyl)indole