{1-[2-(1H-indol-3-yl)-ethyl]-1,2,5,6-tetrahydro-pyridin-3-yl}-acetic acid benzyl ester

Base Information

• Chemical Name: {1-[2-(1H-indol-3-yl)-ethyl]-1,2,5,6-tetrahydro-pyridin-3-yl}-acetic acid benzyl ester
• CAS No.: 1358679-56-7
• Molecular Formula: C₂₄H₂₆N₂O₂
• Molecular Weight: 374.483
• Mol file: 1358679-56-7.mol

Synonyms:{1-[2-(1H-indol-3-yl)-ethyl]-1,2,5,6-tetrahydro-pyridin-3-yl}-acetic acid benzyl ester

Chemical Property of {1-[2-(1H-indol-3-yl)-ethyl]-1,2,5,6-tetrahydro-pyridin-3-yl}-acetic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of {1-[2-(1H-indol-3-yl)-ethyl]-1,2,5,6-tetrahydro-pyridin-3-yl}-acetic acid benzyl ester

There total 3 articles about {1-[2-(1H-indol-3-yl)-ethyl]-1,2,5,6-tetrahydro-pyridin-3-yl}-acetic acid benzyl 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: 80.0%

3-benzyloxycarbonylmethyl-1-[2-(1H-indol-3-yl)-ethyl]-pyridinium bromide (1358679-75-0) → {1-[2-(1H-indol-3-yl)-ethyl]-1,2,5,6-tetrahydro-pyridin-3-yl}-acetic acid benzyl ester (1358679-56-7)

Guidance literature:

With sodium tetrahydroborate; In methanol; at 0 - 20 ℃; for 20h; Inert atmosphere;

DOI:10.1002/ejoc.201101058

Reference yield:

3-(2-bromoethyl)-1H-indole (3389-21-7) → {1-[2-(1H-indol-3-yl)-ethyl]-1,2,5,6-tetrahydro-pyridin-3-yl}-acetic acid benzyl ester (1358679-56-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 3 h / 80 °C / Inert atmosphere; Neat (no solvent)

2: sodium tetrahydroborate / methanol / 20 h / 0 - 20 °C / Inert atmosphere

With sodium tetrahydroborate; In methanol;

DOI:10.1002/ejoc.201101058

Reference yield:

pyridin-3-yl-acetic acid benzyl ester (170583-11-6) → {1-[2-(1H-indol-3-yl)-ethyl]-1,2,5,6-tetrahydro-pyridin-3-yl}-acetic acid benzyl ester (1358679-56-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 3 h / 80 °C / Inert atmosphere; Neat (no solvent)

2: sodium tetrahydroborate / methanol / 20 h / 0 - 20 °C / Inert atmosphere

With sodium tetrahydroborate; In methanol;

DOI:10.1002/ejoc.201101058

upstream raw materials:

3-(2-bromoethyl)-1H-indole

pyridin-3-yl-acetic acid benzyl ester

3-benzyloxycarbonylmethyl-1-[2-(1H-indol-3-yl)-ethyl]-pyridinium bromide