2-Amino-3-(5-benzyloxy-1H-indol-3-yl)-N,N-dipentyl-propionamide; hydrochloride

Base Information

Chemical Name:2-Amino-3-(5-benzyloxy-1H-indol-3-yl)-N,N-dipentyl-propionamide; hydrochloride
CAS No.:136631-74-8
Molecular Formula:C₂₈H₃₉N₃O₂*ClH
Molecular Weight:486.097
Hs Code.:

Synonyms:2-Amino-3-(5-benzyloxy-1H-indol-3-yl)-N,N-dipentyl-propionamide; hydrochloride

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Chemical Property of 2-Amino-3-(5-benzyloxy-1H-indol-3-yl)-N,N-dipentyl-propionamide; hydrochloride

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Technology Process of 2-Amino-3-(5-benzyloxy-1H-indol-3-yl)-N,N-dipentyl-propionamide; hydrochloride

There total 3 articles about 2-Amino-3-(5-benzyloxy-1H-indol-3-yl)-N,N-dipentyl-propionamide; hydrochloride 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:

: 127369-33-9
[2-(5-Benzyloxy-1H-indol-3-yl)-1-dipentylcarbamoyl-ethyl]-carbamic acid tert-butyl ester

: 136631-74-8
2-Amino-3-(5-benzyloxy-1H-indol-3-yl)-N,N-dipentyl-propionamide; hydrochloride

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; for 1h;
DOI:10.1021/jm00116a002

Reference yield:

: 1956-25-8
5-Benzyloxy-tryptophan

: 136631-74-8
2-Amino-3-(5-benzyloxy-1H-indol-3-yl)-N,N-dipentyl-propionamide; hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 2.) bis(2-oxo-3-oxazolidinyl)phosphinic acid (BOPCl), triethylamine (TEA) / 2.) CH₂Cl₂, from 0 deg C, to RT

2: 4 N HCl / dioxane / 1 h

With hydrogenchloride; bis(2-oxo-3-oxazolidinyl)-phosphinic acid; triethylamine; In 1,4-dioxane;
DOI:10.1021/jm00116a002

Reference yield:

: 2050-92-2
Di-n-amylamine

: 136631-74-8
2-Amino-3-(5-benzyloxy-1H-indol-3-yl)-N,N-dipentyl-propionamide; hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 2.) bis(2-oxo-3-oxazolidinyl)phosphinic acid (BOPCl), triethylamine (TEA) / 2.) CH₂Cl₂, from 0 deg C, to RT

2: 4 N HCl / dioxane / 1 h

With hydrogenchloride; bis(2-oxo-3-oxazolidinyl)-phosphinic acid; triethylamine; In 1,4-dioxane;
DOI:10.1021/jm00116a002