1H-Imidazole-1-ethanol, a-(4-methoxyphenyl)-a-[4

Base Information

• Chemical Name: 1H-Imidazole-1-ethanol, a-(4-methoxyphenyl)-a-[4
• CAS No.: 137103-63-0
• Molecular Formula: C23H21N3O2
• Molecular Weight: 371.439
• ChEMBL ID: CHEMBL323041
• DSSTox Substance ID: DTXSID70875424
• Nikkaji Number: J491.824J

Synonyms:137103-63-0;CHEMBL323041;SCHEMBL9199981;DTXSID70875424;1H-Imidazole-1-ethanol, a-(4-methoxyphenyl)-a-[4

Chemical Property of 1H-Imidazole-1-ethanol, a-(4-methoxyphenyl)-a-[4

Chemical Property:

• XLogP3: 2.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 6
• Exact Mass: 371.16337692
• Heavy Atom Count: 28
• Complexity: 469

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: COC1=CC=C(C=C1)C(CN2C=CN=C2)(C3=CC=C(C=C3)C4=CC=NC=C4)O

Technology Process of 1H-Imidazole-1-ethanol, a-(4-methoxyphenyl)-a-[4

There total 4 articles about 1H-Imidazole-1-ethanol, a-(4-methoxyphenyl)-a-[4 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: 19.0%

4-trimethylstannyl-pyridine (59020-06-3) + 1-(4-Bromo-phenyl)-2-imidazol-1-yl-1-(4-methoxy-phenyl)-ethanol (142657-47-4) → 1-(4-methoxyphenyl)-1-[4-(pyridin-4-yl)phenyl]-2-(1-imidazolyl)ethanol (137103-63-0)

Guidance literature:

With bis-triphenylphosphine-palladium(II) chloride; triethylamine; In N,N-dimethyl-formamide; at 70 ℃;

DOI:10.1021/jm00095a009

Reference yield:

4-bromophenyllithium (22480-64-4) → 1-(4-methoxyphenyl)-1-[4-(pyridin-4-yl)phenyl]-2-(1-imidazolyl)ethanol (137103-63-0)

Guidance literature:

Multi-step reaction with 3 steps

1: tetrahydrofuran / -78 °C

2: 5 percent / t-BuOK / dimethylformamide / 90 °C

3: 19 percent / Et₃N, Pd(PPh₃)2Cl₂ / dimethylformamide / 70 °C

With bis-triphenylphosphine-palladium(II) chloride; potassium tert-butylate; triethylamine; In tetrahydrofuran; N,N-dimethyl-formamide;

DOI:10.1021/jm00095a009

Reference yield:

2-(4-Bromo-phenyl)-2-(4-methoxy-phenyl)-oxirane → 1-(4-methoxyphenyl)-1-[4-(pyridin-4-yl)phenyl]-2-(1-imidazolyl)ethanol (137103-63-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 5 percent / t-BuOK / dimethylformamide / 90 °C

2: 19 percent / Et₃N, Pd(PPh₃)2Cl₂ / dimethylformamide / 70 °C

With bis-triphenylphosphine-palladium(II) chloride; potassium tert-butylate; triethylamine; In N,N-dimethyl-formamide;

DOI:10.1021/jm00095a009

upstream raw materials:

4-trimethylstannyl-pyridine

1-(4-Bromo-phenyl)-2-imidazol-1-yl-1-(4-methoxy-phenyl)-ethanol

4-bromophenyllithium

2-chloro-1-(4-methoxyphenyl)ethanone

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