[1-benzyl-3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrol-2-yl]-(3,3-dimethylpiperazin-1-yl)-methanone

Base Information

Chemical Name:[1-benzyl-3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrol-2-yl]-(3,3-dimethylpiperazin-1-yl)-methanone
CAS No.:1574112-08-5
Molecular Formula:C₂₅H₂₅ClF₃N₃O
Molecular Weight:475.941
Hs Code.:

Synonyms:[1-benzyl-3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrol-2-yl]-(3,3-dimethylpiperazin-1-yl)-methanone

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Chemical Property of [1-benzyl-3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrol-2-yl]-(3,3-dimethylpiperazin-1-yl)-methanone

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Technology Process of [1-benzyl-3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrol-2-yl]-(3,3-dimethylpiperazin-1-yl)-methanone

There total 8 articles about [1-benzyl-3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrol-2-yl]-(3,3-dimethylpiperazin-1-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: 67.0%

: 1574118-74-3
tert-butyl 4-(1-benzyl-3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-2-carbonyl)-2,2-dimethylpiperazine-1-carboxylate

: 1574112-08-5
[1-benzyl-3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrol-2-yl]-(3,3-dimethylpiperazin-1-yl)-methanone

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 0 ℃; for 1h;

Reference yield:

: 1-chloro-4-(1-iodo-2-tosylethyl)benzene

: 1574112-08-5
[1-benzyl-3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrol-2-yl]-(3,3-dimethylpiperazin-1-yl)-methanone

Guidance literature:: Multi-step reaction with 7 steps

1.1: triethylamine / acetonitrile / 1 h / 20 °C

2.1: sodium hydride / tetrahydrofuran; mineral oil / 0.08 h / 0 °C / Inert atmosphere

2.2: 18 h / 20 °C

3.1: dichlortris(1,10-phenanthroline)-ruthenium(II) hydrate; dipotassium hydrogenphosphate / acetonitrile / 16 h / 20 °C / Inert atmosphere

4.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 1 h / 20 °C

5.1: sodium hydroxide / tetrahydrofuran; water / 7 h / 80 - 100 °C

6.1: N-ethyl-N,N-diisopropylamine; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride / 1,2-dimethoxyethane / 3 h / 60 °C

7.1: trifluoroacetic acid / dichloromethane / 1 h / 0 °C

With dipotassium hydrogenphosphate; di-isopropyl azodicarboxylate; dichlortris(1,10-phenanthroline)-ruthenium(II) hydrate; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; sodium hydride; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; water; acetonitrile; mineral oil;

Reference yield:

: 1574117-40-0
ethyl 3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-2-carboxylate

: 1574112-08-5
[1-benzyl-3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrol-2-yl]-(3,3-dimethylpiperazin-1-yl)-methanone

Guidance literature:: Multi-step reaction with 4 steps

1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 1 h / 20 °C

2: sodium hydroxide / tetrahydrofuran; water / 7 h / 80 - 100 °C

3: N-ethyl-N,N-diisopropylamine; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride / 1,2-dimethoxyethane / 3 h / 60 °C

4: trifluoroacetic acid / dichloromethane / 1 h / 0 °C

With di-isopropyl azodicarboxylate; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; N-ethyl-N,N-diisopropylamine; triphenylphosphine; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; water;