(5-(4-(benzyloxy)phenyl)-3-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl)(2-chloro-6-methylpyridin-3-yl)methanone

Base Information

• Chemical Name: (5-(4-(benzyloxy)phenyl)-3-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl)(2-chloro-6-methylpyridin-3-yl)methanone
• CAS No.: 1381883-44-8
• Molecular Formula: C₃₀H₂₆ClN₃O₃
• Molecular Weight: 512.008
• Mol file: 1381883-44-8.mol

Synonyms:(5-(4-(benzyloxy)phenyl)-3-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl)(2-chloro-6-methylpyridin-3-yl)methanone

Chemical Property of (5-(4-(benzyloxy)phenyl)-3-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl)(2-chloro-6-methylpyridin-3-yl)methanone

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (5-(4-(benzyloxy)phenyl)-3-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl)(2-chloro-6-methylpyridin-3-yl)methanone

There total 5 articles about (5-(4-(benzyloxy)phenyl)-3-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl)(2-chloro-6-methylpyridin-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: 79.0%

C23H22N2O2 (1381883-25-5) + 2-chloro-6-methyl nicotinic acid (30529-70-5) → (5-(4-(benzyloxy)phenyl)-3-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl)(2-chloro-6-methylpyridin-3-yl)methanone (1381883-44-8)

Guidance literature:

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; for 8h; Reflux;

DOI:10.1016/j.bmc.2012.04.047

Reference yield: 79.0%

→ (5-(4-(benzyloxy)phenyl)-3-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl)(2-chloro-6-methylpyridin-3-yl)methanone (1381883-44-8)

Guidance literature:

With hydrazine hydrate; In propan-1-ol; at 90 ℃; for 10h;

With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 45 ℃; for 12h;

Reference yield:

p-benzyloxybenzaldehyde (4397-53-9) → (5-(4-(benzyloxy)phenyl)-3-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl)(2-chloro-6-methylpyridin-3-yl)methanone (1381883-44-8)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium hydroxide / ethanol / 20 °C

2: hydrazine hydrate / isopropyl alcohol / 8 h / Reflux

3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 8 h / Reflux

With benzotriazol-1-ol; hydrazine hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; potassium hydroxide; In ethanol; dichloromethane; isopropyl alcohol;

DOI:10.1016/j.bmc.2012.04.047

upstream raw materials:

p-benzyloxybenzaldehyde

C₂₃H₂₀O₃

C₂₃H₂₂N₂O₂

2-chloro-6-methyl nicotinic acid