[1-(1-benzyl-piperidin-4-yl)-1H-indol-3-yl]-oxo-acetic acid methyl ester

Base Information

Chemical Name:[1-(1-benzyl-piperidin-4-yl)-1H-indol-3-yl]-oxo-acetic acid methyl ester
CAS No.:604009-20-3
Molecular Formula:C₂₃H₂₄N₂O₃
Molecular Weight:376.455
Hs Code.:

Synonyms:[1-(1-benzyl-piperidin-4-yl)-1H-indol-3-yl]-oxo-acetic acid methyl ester

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Chemical Property of [1-(1-benzyl-piperidin-4-yl)-1H-indol-3-yl]-oxo-acetic acid methyl ester

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Technology Process of [1-(1-benzyl-piperidin-4-yl)-1H-indol-3-yl]-oxo-acetic acid methyl ester

There total 4 articles about [1-(1-benzyl-piperidin-4-yl)-1H-indol-3-yl]-oxo-acetic acid methyl ester 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: 94.0%

: 67-56-1
methanol

: 79-37-8
oxalyl dichloride

: 170365-11-4
1-(1-Benzyl-piperidin-4-yl)-1H-indole

: 604009-20-3
[1-(1-benzyl-piperidin-4-yl)-1H-indol-3-yl]-oxo-acetic acid methyl ester

Guidance literature:: 1-(1-Benzyl-piperidin-4-yl)-1H-indole; With hydrogenchloride; In acetonitrile; at 0 - 20 ℃; for 1.16667h;

oxalyl dichloride; In acetonitrile; at 0 ℃; for 1h;

methanol; In acetonitrile; at 0 ℃; for 0.5h;
DOI:10.1016/S0040-4020(03)00973-6

Reference yield:

: 32989-69-8
trans-2-nitro-β-pyrrolidinostyrene

: 604009-20-3
[1-(1-benzyl-piperidin-4-yl)-1H-indol-3-yl]-oxo-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 84 percent / TMSCl / 22 h / Heating

2.1: 100 percent / H₂ / Pd/C / methanol / 20 °C / 1034.3 - 2585.74 Torr

3.1: 83 percent / NaBH(OAc)3 / acetic acid / 19 h / 20 - 50 °C

4.1: HCl / acetonitrile / 1.17 h / 0 - 20 °C

4.2: acetonitrile / 1 h / 0 °C

4.3: 94 percent / acetonitrile / 0.5 h / 0 °C

With hydrogenchloride; chloro-trimethyl-silane; hydrogen; sodium tris(acetoxy)borohydride; palladium on activated charcoal; In methanol; acetic acid; acetonitrile;
DOI:10.1016/S0040-4020(03)00973-6

Reference yield:

2-(2-nitrophenyl)acetaldehyde dimethyl acetal: 79844-33-0
2-(2-nitrophenyl)acetaldehyde dimethyl acetal

: 604009-20-3
[1-(1-benzyl-piperidin-4-yl)-1H-indol-3-yl]-oxo-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: 100 percent / H₂ / Pd/C / methanol / 20 °C / 1034.3 - 2585.74 Torr

2.1: 83 percent / NaBH(OAc)3 / acetic acid / 19 h / 20 - 50 °C

3.1: HCl / acetonitrile / 1.17 h / 0 - 20 °C

3.2: acetonitrile / 1 h / 0 °C

3.3: 94 percent / acetonitrile / 0.5 h / 0 °C

With hydrogenchloride; hydrogen; sodium tris(acetoxy)borohydride; palladium on activated charcoal; In methanol; acetic acid; acetonitrile;
DOI:10.1016/S0040-4020(03)00973-6