4-[5-(aminomethyl)-1H-indol-2-yl]-6-(4-methylphenyl)-5-pyrimidinol

Base Information

• Chemical Name: 4-[5-(aminomethyl)-1H-indol-2-yl]-6-(4-methylphenyl)-5-pyrimidinol
• CAS No.: 1264924-26-6
• Molecular Formula: C₂₀H₁₈N₄O
• Molecular Weight: 330.389
• Mol file: 1264924-26-6.mol

Synonyms:4-[5-(aminomethyl)-1H-indol-2-yl]-6-(4-methylphenyl)-5-pyrimidinol

Chemical Property of 4-[5-(aminomethyl)-1H-indol-2-yl]-6-(4-methylphenyl)-5-pyrimidinol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-[5-(aminomethyl)-1H-indol-2-yl]-6-(4-methylphenyl)-5-pyrimidinol

There total 4 articles about 4-[5-(aminomethyl)-1H-indol-2-yl]-6-(4-methylphenyl)-5-pyrimidinol 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:

5-cyanoindole-2-boronic acid (871329-64-5) → 4-[5-(aminomethyl)-1H-indol-2-yl]-6-(4-methylphenyl)-5-pyrimidinol (1264924-26-6)

Guidance literature:

Multi-step reaction with 4 steps

1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / toluene; 1,2-dimethoxyethane; water / 140 °C / Inert atmosphere; in a pressure tube; microwave reactor

2: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / toluene; 1,2-dimethoxyethane; water / 16 h / 100 °C / Inert atmosphere

3: lithium iodide / quinoline / 0.17 h / 200 °C / Inert atmosphere; sealed in a pressure tube; microwave reactor

4: hydrogen; ammonia / Raney Ni / methanol / 50 °C / 3102.97 Torr / sealed in a pressure tube

With ammonia; hydrogen; potassium carbonate; lithium iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In quinoline; methanol; 1,2-dimethoxyethane; water; toluene;

Reference yield:

C20H14N4O (1264926-36-4) → 4-[5-(aminomethyl)-1H-indol-2-yl]-6-(4-methylphenyl)-5-pyrimidinol (1264924-26-6)

Guidance literature:

With ammonia; hydrogen; Raney Ni; In methanol; at 50 ℃; under 3102.97 Torr; sealed in a pressure tube;

Reference yield:

2-[5-methoxy-6-(4-methylphenyl)-4-pyrimidinyl]-1H-indole-5-carbonitrile (1264924-22-2) → 4-[5-(aminomethyl)-1H-indol-2-yl]-6-(4-methylphenyl)-5-pyrimidinol (1264924-26-6)

Guidance literature:

Multi-step reaction with 2 steps

1: lithium iodide / quinoline / 0.17 h / 200 °C / Inert atmosphere; sealed in a pressure tube; microwave reactor

2: hydrogen; ammonia / Raney Ni / methanol / 50 °C / 3102.97 Torr / sealed in a pressure tube

With ammonia; hydrogen; lithium iodide; Raney Ni; In quinoline; methanol;

upstream raw materials:

5-cyanoindole-2-boronic acid

2-[5-methoxy-6-(4-methylphenyl)-4-pyrimidinyl]-1H-indole-5-carbonitrile

C₁₄H₉ClN₄O

C₂₀H₁₄N₄O