N-(3-(5-(1-ethyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-5-(1H-pyrrol-1-yl)phenyl)acetamide

Base Information

• Chemical Name: N-(3-(5-(1-ethyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-5-(1H-pyrrol-1-yl)phenyl)acetamide
• CAS No.: 1430725-01-1
• Molecular Formula: C₂₄H₂₂N₆O
• Molecular Weight: 410.478
• Mol file: 1430725-01-1.mol

Synonyms:N-(3-(5-(1-ethyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-5-(1H-pyrrol-1-yl)phenyl)acetamide

Chemical Property of N-(3-(5-(1-ethyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-5-(1H-pyrrol-1-yl)phenyl)acetamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-(3-(5-(1-ethyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-5-(1H-pyrrol-1-yl)phenyl)acetamide

There total 9 articles about N-(3-(5-(1-ethyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-5-(1H-pyrrol-1-yl)phenyl)acetamide 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: 74.0%

N-(3-(5-bromo-1H-benzo[d]imidazol-1-yl)-5-(1H-pyrrol-1-yl)phenyl)acetamide (1430727-92-6) + 1-ethyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyrazole (847818-70-6) → N-(3-(5-(1-ethyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-5-(1H-pyrrol-1-yl)phenyl)acetamide (1430725-01-1)

Guidance literature:

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate; In 1,2-dimethoxyethane; water; at 100 ℃; for 2h; Inert atmosphere;

Reference yield:

1-(3,5-dinitro-phenyl)-1H-pyrrole (321329-77-5) → N-(3-(5-(1-ethyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-5-(1H-pyrrol-1-yl)phenyl)acetamide (1430725-01-1)

Guidance literature:

Multi-step reaction with 7 steps

1: diammonium sulfide; pyridine / water; ethanol / 4 h / 80 °C

2: 0.5 h / 20 °C

3: water; calcium chloride; iron / ethanol / 2 h / 80 °C

4: potassium fluoride / N,N-dimethyl-formamide / 110 °C

5: water; calcium chloride; iron / ethanol / 2 h / 80 °C

6: 2 h / 20 - 100 °C

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

With pyridine; diammonium sulfide; potassium fluoride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; water; iron; sodium carbonate; calcium chloride; In 1,2-dimethoxyethane; ethanol; water; N,N-dimethyl-formamide;

Reference yield:

3, 5-dinitroaniline (618-87-1) → N-(3-(5-(1-ethyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-5-(1H-pyrrol-1-yl)phenyl)acetamide (1430725-01-1)

Guidance literature:

Multi-step reaction with 8 steps

1: acetic acid / 16 h / 100 °C

2: diammonium sulfide; pyridine / water; ethanol / 4 h / 80 °C

3: 0.5 h / 20 °C

4: water; calcium chloride; iron / ethanol / 2 h / 80 °C

5: potassium fluoride / N,N-dimethyl-formamide / 110 °C

6: water; calcium chloride; iron / ethanol / 2 h / 80 °C

7: 2 h / 20 - 100 °C

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

With pyridine; diammonium sulfide; potassium fluoride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; water; iron; sodium carbonate; acetic acid; calcium chloride; In 1,2-dimethoxyethane; ethanol; water; N,N-dimethyl-formamide;

upstream raw materials:

1-(3,5-dinitro-phenyl)-1H-pyrrole

3, 5-dinitroaniline

(3-nitro-5-pyrrol-1-yl-phenyl)amine

N-(3-nitro-5-pyrrol-1-yl-phenyl)-acetamide

Downstream raw materials:

3-(5-(1-ethyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-5-(1H-pyrrol-1-yl)aniline

N-(3-(5-(1-ethyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-5-(1H-pyrrol-1-yl)phenyl)ethanesulfonamide