tert-butyl 4-(2-((2-(tert-butyldimethylsilyloxy)ethyl)(naphthalen-1-yl)amino)-2-oxoethyl)phenylcarbamate

Base Information

Chemical Name:tert-butyl 4-(2-((2-(tert-butyldimethylsilyloxy)ethyl)(naphthalen-1-yl)amino)-2-oxoethyl)phenylcarbamate
CAS No.:1350651-85-2
Molecular Formula:C₃₁H₄₂N₂O₄Si
Molecular Weight:534.771
Hs Code.:

Synonyms:tert-butyl 4-(2-((2-(tert-butyldimethylsilyloxy)ethyl)(naphthalen-1-yl)amino)-2-oxoethyl)phenylcarbamate

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Chemical Property of tert-butyl 4-(2-((2-(tert-butyldimethylsilyloxy)ethyl)(naphthalen-1-yl)amino)-2-oxoethyl)phenylcarbamate

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Technology Process of tert-butyl 4-(2-((2-(tert-butyldimethylsilyloxy)ethyl)(naphthalen-1-yl)amino)-2-oxoethyl)phenylcarbamate

There total 4 articles about tert-butyl 4-(2-((2-(tert-butyldimethylsilyloxy)ethyl)(naphthalen-1-yl)amino)-2-oxoethyl)phenylcarbamate 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: 76.0%

: 1350651-81-8
N-(2-(tert-butyldimethylsilyloxy)ethyl)naphthalen-1-amine

: 81196-09-0
2-(4-(tert-butoxycarbonylamino)phenyl)acetic acid

: 1350651-85-2
tert-butyl 4-(2-((2-(tert-butyldimethylsilyloxy)ethyl)(naphthalen-1-yl)amino)-2-oxoethyl)phenylcarbamate

Guidance literature:: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃;

Reference yield:

: 134-32-7
1-amino-naphthalene

: 1350651-85-2
tert-butyl 4-(2-((2-(tert-butyldimethylsilyloxy)ethyl)(naphthalen-1-yl)amino)-2-oxoethyl)phenylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

1: methanol / 20 °C / Inert atmosphere

2: methanol; sodium tetrahydroborate / 0.17 h

3: 1H-imidazole / dichloromethane / 20 °C / Inert atmosphere

4: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

With 1H-imidazole; methanol; sodium tetrahydroborate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In methanol; dichloromethane;

Reference yield:

: 2933-59-7
N-(2-hydroxyethyl)-1-naphthylamine

: 1350651-85-2
tert-butyl 4-(2-((2-(tert-butyldimethylsilyloxy)ethyl)(naphthalen-1-yl)amino)-2-oxoethyl)phenylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: 1H-imidazole / dichloromethane / 20 °C / Inert atmosphere

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

With 1H-imidazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane;