3-{[4-bromo-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-1-yl]methyl}benzonitrile

Base Information

Chemical Name:3-{[4-bromo-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-1-yl]methyl}benzonitrile
CAS No.:1221504-20-6
Molecular Formula:C₁₈H₁₃BrFN₃
Molecular Weight:370.224
Hs Code.:

Synonyms:3-{[4-bromo-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-1-yl]methyl}benzonitrile

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Chemical Property of 3-{[4-bromo-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-1-yl]methyl}benzonitrile

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Technology Process of 3-{[4-bromo-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-1-yl]methyl}benzonitrile

There total 6 articles about 3-{[4-bromo-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-1-yl]methyl}benzonitrile 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:

: 1221504-19-3
3-{[5-(4-fluorophenyl)-3-methyl-1H-pyrazol-1-yl]methyl}benzonitrile

: 1221504-20-6
3-{[4-bromo-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-1-yl]methyl}benzonitrile

Guidance literature:: With N-Bromosuccinimide; In acetonitrile; at 20 ℃; for 1h;

Reference yield:

: 1221504-18-2
3-(hydrazinomethyl)benzonitrile trifluoroacetic acid

: 1221504-20-6
3-{[4-bromo-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-1-yl]methyl}benzonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine; trifluoroacetic acid / isopropyl alcohol / 2 h / 80 °C

2: N-Bromosuccinimide / acetonitrile / 1 h / 20 °C

With N-Bromosuccinimide; triethylamine; trifluoroacetic acid; In isopropyl alcohol; acetonitrile;

Reference yield:

: 24964-64-5
3-Cyanobenzaldehyde

: 1221504-20-6
3-{[4-bromo-5-(4-fluorophenyl)-3-methyl-1H-pyrazol-1-yl]methyl}benzonitrile

Guidance literature:: Multi-step reaction with 5 steps

1: ethanol / 3 h / 20 °C

2: sodium cyanoborohydride; acetic acid / water / 2 h / 20 °C

3: dichloromethane / 20 °C

4: triethylamine; trifluoroacetic acid / isopropyl alcohol / 2 h / 80 °C

5: N-Bromosuccinimide / acetonitrile / 1 h / 20 °C

With N-Bromosuccinimide; sodium cyanoborohydride; acetic acid; triethylamine; trifluoroacetic acid; In ethanol; dichloromethane; water; isopropyl alcohol; acetonitrile;