di-tert-butyl 2,2'-(2-(2-(2-((2-(2-(4,10-bis(2-tert-butoxy-2-oxoethyl)-7-(2-oxo-2-(2-(trifluoromethyl)phenylamino)ethyl)-1,4,7,10-tetraazacyclododecan-1-yl)ethylamino)-2-oxoethyl)(2-tert-butoxy-2-oxoethyl)amino)ethoxy)phenoxy)ethylazanediyl)diacetate

Base Information

Chemical Name:di-tert-butyl 2,2'-(2-(2-(2-((2-(2-(4,10-bis(2-tert-butoxy-2-oxoethyl)-7-(2-oxo-2-(2-(trifluoromethyl)phenylamino)ethyl)-1,4,7,10-tetraazacyclododecan-1-yl)ethylamino)-2-oxoethyl)(2-tert-butoxy-2-oxoethyl)amino)ethoxy)phenoxy)ethylazanediyl)diacetate
CAS No.:1402393-82-1
Molecular Formula:C₆₁H₉₇F₃N₈O₁₄
Molecular Weight:1223.48
Hs Code.:

di-tert-butyl 2,2'-(2-(2-(2-((2-(2-(4,10-bis(2-tert-butoxy-2-oxoethyl)-7-(2-oxo-2-(2-(trifluoromethyl)phenylamino)ethyl)-1,4,7,10-tetraazacyclododecan-1-yl)ethylamino)-2-oxoethyl)(2-tert-butoxy-2-oxoethyl)amino)ethoxy)phenoxy)ethylazanediyl)diacetate

Synonyms:di-tert-butyl 2,2'-(2-(2-(2-((2-(2-(4,10-bis(2-tert-butoxy-2-oxoethyl)-7-(2-oxo-2-(2-(trifluoromethyl)phenylamino)ethyl)-1,4,7,10-tetraazacyclododecan-1-yl)ethylamino)-2-oxoethyl)(2-tert-butoxy-2-oxoethyl)amino)ethoxy)phenoxy)ethylazanediyl)diacetate

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Chemical Property of di-tert-butyl 2,2'-(2-(2-(2-((2-(2-(4,10-bis(2-tert-butoxy-2-oxoethyl)-7-(2-oxo-2-(2-(trifluoromethyl)phenylamino)ethyl)-1,4,7,10-tetraazacyclododecan-1-yl)ethylamino)-2-oxoethyl)(2-tert-butoxy-2-oxoethyl)amino)ethoxy)phenoxy)ethylazanediyl)diacetate

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Technology Process of di-tert-butyl 2,2'-(2-(2-(2-((2-(2-(4,10-bis(2-tert-butoxy-2-oxoethyl)-7-(2-oxo-2-(2-(trifluoromethyl)phenylamino)ethyl)-1,4,7,10-tetraazacyclododecan-1-yl)ethylamino)-2-oxoethyl)(2-tert-butoxy-2-oxoethyl)amino)ethoxy)phenoxy)ethylazanediyl)diacetate

There total 5 articles about di-tert-butyl 2,2'-(2-(2-(2-((2-(2-(4,10-bis(2-tert-butoxy-2-oxoethyl)-7-(2-oxo-2-(2-(trifluoromethyl)phenylamino)ethyl)-1,4,7,10-tetraazacyclododecan-1-yl)ethylamino)-2-oxoethyl)(2-tert-butoxy-2-oxoethyl)amino)ethoxy)phenoxy)ethylazanediyl)diacetate 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: 20.0%

: 1278587-14-6
2-((2-(2-(2-(bis(2-tert-butoxy-2-oxoethyl)amino)ethoxy)phenoxy)ethyl)(2-tert-butoxy-2-oxoethyl)amino)acetic acid

: 1402393-81-0
di-tert-butyl 2,2'-(4-(2-aminoethyl)-10-(2-oxo-2-(2-(trifluoromethyl)phenylamino)ethyl)-1,4,7,10-tetraazacyclododecane-1,7-diyl)diacetate

: 1402393-82-1
di-tert-butyl 2,2'-(2-(2-(2-((2-(2-(4,10-bis(2-tert-butoxy-2-oxoethyl)-7-(2-oxo-2-(2-(trifluoromethyl)phenylamino)ethyl)-1,4,7,10-tetraazacyclododecan-1-yl)ethylamino)-2-oxoethyl)(2-tert-butoxy-2-oxoethyl)amino)ethoxy)phenoxy)ethylazanediyl)diacetate

Guidance literature:: 2-((2-(2-(2-(bis(2-tert-butoxy-2-oxoethyl)amino)ethoxy)phenoxy)ethyl)(2-tert-butoxy-2-oxoethyl)amino)acetic acid; di-tert-butyl 2,2'-(4-(2-aminoethyl)-10-(2-oxo-2-(2-(trifluoromethyl)phenylamino)ethyl)-1,4,7,10-tetraazacyclododecane-1,7-diyl)diacetate; With 4-methyl-morpholine; benzotriazol-1-ol; In N,N-dimethyl-formamide; at 0 - 5 ℃; for 0.25h;

With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1002/chem.201200737

Reference yield:

: 3792-04-9
2-chloro-N-[2-(trifluoromethyl)phenyl]acetamide

: 1402393-82-1
di-tert-butyl 2,2'-(2-(2-(2-((2-(2-(4,10-bis(2-tert-butoxy-2-oxoethyl)-7-(2-oxo-2-(2-(trifluoromethyl)phenylamino)ethyl)-1,4,7,10-tetraazacyclododecan-1-yl)ethylamino)-2-oxoethyl)(2-tert-butoxy-2-oxoethyl)amino)ethoxy)phenoxy)ethylazanediyl)diacetate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium carbonate / acetonitrile / 0.5 h / 20 °C / Inert atmosphere

1.2: 80 °C / Inert atmosphere

2.1: potassium carbonate / acetonitrile / 0.5 h / 20 °C / Inert atmosphere

2.2: Inert atmosphere; Reflux

3.1: palladium 10% on activated carbon; hydrogen / methanol / 8 h / 20 °C / 2068.65 Torr

4.1: 4-methyl-morpholine; benzotriazol-1-ol / N,N-dimethyl-formamide / 0.25 h / 0 - 5 °C

4.2: 20 °C

With 4-methyl-morpholine; palladium 10% on activated carbon; hydrogen; sodium carbonate; potassium carbonate; benzotriazol-1-ol; In methanol; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1002/chem.201200737

Reference yield:

: 1402393-78-5
di-tert-butyl 2,2'-(4-(2-oxo-2-(2-(trifluoromethyl)phenylamino)ethyl)-1,4,7,10-tetraazacyclododecane-1,7-diyl)diacetate

: 1402393-82-1
di-tert-butyl 2,2'-(2-(2-(2-((2-(2-(4,10-bis(2-tert-butoxy-2-oxoethyl)-7-(2-oxo-2-(2-(trifluoromethyl)phenylamino)ethyl)-1,4,7,10-tetraazacyclododecan-1-yl)ethylamino)-2-oxoethyl)(2-tert-butoxy-2-oxoethyl)amino)ethoxy)phenoxy)ethylazanediyl)diacetate

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / acetonitrile / 0.5 h / 20 °C / Inert atmosphere

1.2: Inert atmosphere; Reflux

2.1: palladium 10% on activated carbon; hydrogen / methanol / 8 h / 20 °C / 2068.65 Torr

3.1: 4-methyl-morpholine; benzotriazol-1-ol / N,N-dimethyl-formamide / 0.25 h / 0 - 5 °C

3.2: 20 °C

With 4-methyl-morpholine; palladium 10% on activated carbon; hydrogen; potassium carbonate; benzotriazol-1-ol; In methanol; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1002/chem.201200737