1-[5-(piperidin-1-yl)-2-(4-benzyloxybenzoylamino)phenyl]-3-phenylpropan-1-one

Base Information

Chemical Name:1-[5-(piperidin-1-yl)-2-(4-benzyloxybenzoylamino)phenyl]-3-phenylpropan-1-one
CAS No.:1339010-20-6
Molecular Formula:C₃₄H₃₄N₂O₃
Molecular Weight:518.656
Hs Code.:

Synonyms:1-[5-(piperidin-1-yl)-2-(4-benzyloxybenzoylamino)phenyl]-3-phenylpropan-1-one

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Chemical Property of 1-[5-(piperidin-1-yl)-2-(4-benzyloxybenzoylamino)phenyl]-3-phenylpropan-1-one

Chemical Property:

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Technology Process of 1-[5-(piperidin-1-yl)-2-(4-benzyloxybenzoylamino)phenyl]-3-phenylpropan-1-one

There total 4 articles about 1-[5-(piperidin-1-yl)-2-(4-benzyloxybenzoylamino)phenyl]-3-phenylpropan-1-one 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:

: 1339010-05-7
1-[5-(piperidin-1-yl)-2-nitrophenyl]-3-phenylprop-2-en-1-one

: 1339010-20-6
1-[5-(piperidin-1-yl)-2-(4-benzyloxybenzoylamino)phenyl]-3-phenylpropan-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: palladium 10% on activated carbon; hydrogen / methanol; ethyl acetate / 4 h / 20 °C

2: triethylamine / tetrahydrofuran / 2 h / 0 °C

With palladium 10% on activated carbon; hydrogen; triethylamine; In tetrahydrofuran; methanol; ethyl acetate;
DOI:10.1016/j.bmc.2011.07.029

Reference yield:

: 56915-86-7
2'-nitro-5'-(piperidin-1-yl)acetophenone

: 1339010-20-6
1-[5-(piperidin-1-yl)-2-(4-benzyloxybenzoylamino)phenyl]-3-phenylpropan-1-one

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide / ethanol; water / 2 h / 20 °C

2: palladium 10% on activated carbon; hydrogen / methanol; ethyl acetate / 4 h / 20 °C

3: triethylamine / tetrahydrofuran / 2 h / 0 °C

With palladium 10% on activated carbon; hydrogen; triethylamine; sodium hydroxide; In tetrahydrofuran; methanol; ethanol; water; ethyl acetate;
DOI:10.1016/j.bmc.2011.07.029

Reference yield:

: 18640-60-3
5-chloro-2-nitroacetophenone

: 1339010-20-6
1-[5-(piperidin-1-yl)-2-(4-benzyloxybenzoylamino)phenyl]-3-phenylpropan-1-one

Guidance literature:: Multi-step reaction with 4 steps

1: N,N-dimethyl-formamide / 4.5 h / 110 °C

2: sodium hydroxide / ethanol; water / 2 h / 20 °C

3: palladium 10% on activated carbon; hydrogen / methanol; ethyl acetate / 4 h / 20 °C

4: triethylamine / tetrahydrofuran / 2 h / 0 °C

With palladium 10% on activated carbon; hydrogen; triethylamine; sodium hydroxide; In tetrahydrofuran; methanol; ethanol; water; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2011.07.029