{1-[2-(1H-indol-3-yl)ethyl]-2,6-dioxopiperidin-3-yl}carbamic acid benzyl ester

Base Information

• Chemical Name: {1-[2-(1H-indol-3-yl)ethyl]-2,6-dioxopiperidin-3-yl}carbamic acid benzyl ester
• CAS No.: 256512-42-2
• Molecular Formula: C₂₃H₂₃N₃O₄
• Molecular Weight: 405.453
• Mol file: 256512-42-2.mol

Synonyms:{1-[2-(1H-indol-3-yl)ethyl]-2,6-dioxopiperidin-3-yl}carbamic acid benzyl ester

Chemical Property of {1-[2-(1H-indol-3-yl)ethyl]-2,6-dioxopiperidin-3-yl}carbamic 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]-2,6-dioxopiperidin-3-yl}carbamic acid benzyl ester

There total 1 articles about {1-[2-(1H-indol-3-yl)ethyl]-2,6-dioxopiperidin-3-yl}carbamic 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: 67.0%

tryptamine (61-54-1) + N-benzyloxycarbonyl-L-glutamic acid (1155-62-0) → {1-[2-(1H-indol-3-yl)ethyl]-2,6-dioxopiperidin-3-yl}carbamic acid benzyl ester (256512-42-2)

Guidance literature:

N-benzyloxycarbonyl-L-glutamic acid; With dmap; TEA; dicyclohexyl-carbodiimide; In tetrahydrofuran; at 0 ℃; for 1h;

tryptamine; With dicyclohexyl-carbodiimide; In dichloromethane; at 0 - 20 ℃; for 24h;

DOI:10.1016/S0040-4039(99)01922-X

Reference yield:

{1-[2-(1H-indol-3-yl)ethyl]-2,6-dioxopiperidin-3-yl}carbamic acid benzyl ester (256512-42-2) → (5S)-5-(benzyloxycarbonyl)amino-6-hydroxy-1-[2-(indol-3-yl)ethyl]piperidin-2-one

Guidance literature:

With hydrogenchloride; sodium tetrahydroborate; In ethanol; pH=8;

DOI:10.1016/S0040-4039(99)01922-X

Reference yield:

{1-[2-(1H-indol-3-yl)ethyl]-2,6-dioxopiperidin-3-yl}carbamic acid benzyl ester (256512-42-2) → (1R,12bR)-(1,2,3,4,6,7,12,12b-Octahydro-indolo[2,3-a]quinolizin-1-yl)-carbamic acid benzyl ester

Guidance literature:

Multi-step reaction with 3 steps

1: NaBH₄; HCl / ethanol / pH 8

2: TFA / CH₂Cl₂ / 2 h / 20 °C

3: 45 percent / LiAlH₄ / tetrahydrofuran / 24 h / 20 °C

With hydrogenchloride; sodium tetrahydroborate; lithium aluminium tetrahydride; trifluoroacetic acid; In tetrahydrofuran; ethanol; dichloromethane; 1: Reduction / 2: Elimination / 3: Reduction;

DOI:10.1016/S0040-4039(99)01922-X

upstream raw materials:

tryptamine

N-benzyloxycarbonyl-L-glutamic acid