4-[(4-allyl-2,5-dimethyl-piperazin-1-yl)-(3-hydroxy-phenyl)-methyl]-N-ethyl-N-phenyl-benzamide

Base Information

Chemical Name:4-[(4-allyl-2,5-dimethyl-piperazin-1-yl)-(3-hydroxy-phenyl)-methyl]-N-ethyl-N-phenyl-benzamide
CAS No.:738578-91-1
Molecular Formula:C₃₁H₃₇N₃O₂
Molecular Weight:483.654
Hs Code.:

4-[(4-allyl-2,5-dimethyl-piperazin-1-yl)-(3-hydroxy-phenyl)-methyl]-<i>N</i>-ethyl-<i>N</i>-phenyl-benzamide

Synonyms:4-[(4-allyl-2,5-dimethyl-piperazin-1-yl)-(3-hydroxy-phenyl)-methyl]-N-ethyl-N-phenyl-benzamide

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Chemical Property of 4-[(4-allyl-2,5-dimethyl-piperazin-1-yl)-(3-hydroxy-phenyl)-methyl]-N-ethyl-N-phenyl-benzamide

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Technology Process of 4-[(4-allyl-2,5-dimethyl-piperazin-1-yl)-(3-hydroxy-phenyl)-methyl]-N-ethyl-N-phenyl-benzamide

There total 6 articles about 4-[(4-allyl-2,5-dimethyl-piperazin-1-yl)-(3-hydroxy-phenyl)-methyl]-N-ethyl-N-phenyl-benzamide 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: 52.0%

: 668490-31-1
4-[(4-allyl-2,5-dimethyl-piperazin-1-yl)-(3-methoxy-phenyl)-methyl]-N-ethyl-N-phenyl-benzamide

: 738578-91-1
4-[(4-allyl-2,5-dimethyl-piperazin-1-yl)-(3-hydroxy-phenyl)-methyl]-N-ethyl-N-phenyl-benzamide

Guidance literature:: With boron tribromide-dimethyl sulfide complex; In dichloromethane; 1,2-dichloro-ethane; at 60 ℃; for 3.5h;
DOI:10.1016/S0968-0896(03)00496-6

Reference yield:

: 619-66-9
4-Carboxybenzaldehyde

: 738578-91-1
4-[(4-allyl-2,5-dimethyl-piperazin-1-yl)-(3-hydroxy-phenyl)-methyl]-N-ethyl-N-phenyl-benzamide

Guidance literature:: Multi-step reaction with 6 steps

1: 88 percent / EDCI / CH₂Cl₂ / 16 h / 20 °C

2: 78 percent / tetrahydrofuran / 10 - 20 °C

3: 97 percent / hydrochloric acid / CHCl₃ / 16 h / 20 °C

4: 72 percent / NaHCO₃ / acetonitrile / 16 h / Heating

5: NaHCO₃ / dimethylformamide / 2 h / 80 °C

6: 52 percent / BBr₃*Me₂S / 1,2-dichloro-ethane; CH₂Cl₂ / 3.5 h / 60 °C

With hydrogenchloride; boron tribromide-dimethyl sulfide complex; sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; dichloromethane; chloroform; 1,2-dichloro-ethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/S0968-0896(03)00496-6

Reference yield:

: 103-69-5
N-ethyl-N-phenylamine

: 738578-91-1
4-[(4-allyl-2,5-dimethyl-piperazin-1-yl)-(3-hydroxy-phenyl)-methyl]-N-ethyl-N-phenyl-benzamide

Guidance literature:: Multi-step reaction with 6 steps

1: 88 percent / EDCI / CH₂Cl₂ / 16 h / 20 °C

2: 78 percent / tetrahydrofuran / 10 - 20 °C

3: 97 percent / hydrochloric acid / CHCl₃ / 16 h / 20 °C

4: 72 percent / NaHCO₃ / acetonitrile / 16 h / Heating

5: NaHCO₃ / dimethylformamide / 2 h / 80 °C

6: 52 percent / BBr₃*Me₂S / 1,2-dichloro-ethane; CH₂Cl₂ / 3.5 h / 60 °C

With hydrogenchloride; boron tribromide-dimethyl sulfide complex; sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; dichloromethane; chloroform; 1,2-dichloro-ethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/S0968-0896(03)00496-6