N-(tert-butyloxycarbonyl)-1,1,1-tris(4-maleimidobenzoyloxymethyl)methylamine

Base Information

Chemical Name:N-(tert-butyloxycarbonyl)-1,1,1-tris(4-maleimidobenzoyloxymethyl)methylamine
CAS No.:927824-76-8
Molecular Formula:C₄₂H₃₄N₄O₁₄
Molecular Weight:818.75
Hs Code.:

Synonyms:N-(tert-butyloxycarbonyl)-1,1,1-tris(4-maleimidobenzoyloxymethyl)methylamine

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Chemical Property of N-(tert-butyloxycarbonyl)-1,1,1-tris(4-maleimidobenzoyloxymethyl)methylamine

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Technology Process of N-(tert-butyloxycarbonyl)-1,1,1-tris(4-maleimidobenzoyloxymethyl)methylamine

There total 3 articles about N-(tert-butyloxycarbonyl)-1,1,1-tris(4-maleimidobenzoyloxymethyl)methylamine 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:

: 24424-99-5
di-tert-butyl dicarbonate

: 927824-76-8
N-(tert-butyloxycarbonyl)-1,1,1-tris(4-maleimidobenzoyloxymethyl)methylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / tetrahydrofuran / 96 h / 20 °C

2: 6.9 g / Et₃N; tert-butyl catechol / 18 h / 20 °C

With t-butyl pyrocatechol; triethylamine; In tetrahydrofuran;
DOI:10.1039/b609500c

Reference yield:

: 29305-46-2
4-(2,5-dioxo-2,5-dihydro-1-pyrrol-1-yl)benzoyl chloride

: 146651-71-0
N-(tert-butyloxycarbonyl)-2-amino-2-(hydroxymethyl)propane-1,3-diol

: 927824-76-8
N-(tert-butyloxycarbonyl)-1,1,1-tris(4-maleimidobenzoyloxymethyl)methylamine

Guidance literature:: With t-butyl pyrocatechol; triethylamine; at 20 ℃; for 18h;
DOI:10.1039/b609500c

Reference yield:

: 17057-04-4
N-(4-carboxyphenyl)maleimide

: 927824-76-8
N-(tert-butyloxycarbonyl)-1,1,1-tris(4-maleimidobenzoyloxymethyl)methylamine

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride; tert-butyl catechol / 2 h / Heating

2: 6.9 g / Et₃N; tert-butyl catechol / 18 h / 20 °C

With thionyl chloride; t-butyl pyrocatechol; triethylamine;
DOI:10.1039/b609500c