2,5,7,10-Tetraazadodec-5-enoic acid, 11-(4,4-dimethyl-2,6-dioxocyclohexylidene)-6-[[(4-methylphenyl)sulfonyl] amino]-12-phenyl-, 1,1-dimethylethyl ester

Base Information

Chemical Name:2,5,7,10-Tetraazadodec-5-enoic acid, 11-(4,4-dimethyl-2,6-dioxocyclohexylidene)-6-[[(4-methylphenyl)sulfonyl] amino]-12-phenyl-, 1,1-dimethylethyl ester
CAS No.:879880-71-4
Molecular Formula:C₃₃H₄₅N₅O₆S
Molecular Weight:639.816
Hs Code.:

2,5,7,10-Tetraazadodec-5-enoic acid,
11-(4,4-dimethyl-2,6-dioxocyclohexylidene)-6-[[(4-methylphenyl)sulfonyl]
amino]-12-phenyl-, 1,1-dimethylethyl ester

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Chemical Property of 2,5,7,10-Tetraazadodec-5-enoic acid, 11-(4,4-dimethyl-2,6-dioxocyclohexylidene)-6-[[(4-methylphenyl)sulfonyl] amino]-12-phenyl-, 1,1-dimethylethyl ester

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Technology Process of 2,5,7,10-Tetraazadodec-5-enoic acid, 11-(4,4-dimethyl-2,6-dioxocyclohexylidene)-6-[[(4-methylphenyl)sulfonyl] amino]-12-phenyl-, 1,1-dimethylethyl ester

There total 3 articles about 2,5,7,10-Tetraazadodec-5-enoic acid, 11-(4,4-dimethyl-2,6-dioxocyclohexylidene)-6-[[(4-methylphenyl)sulfonyl] amino]-12-phenyl-, 1,1-dimethylethyl 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:

: [1-(2-tert-Butoxycarbonylamino-ethylamino)-1-{2-[1-(4,4-dimethyl-2,6-dioxo-cyclohexylidene)-2-phenyl-ethylamino]-ethylamino}-meth-(E)-ylidene]-methyl-sulfonium; iodide

: 879880-71-4
(2-{[{2-[1-(4,4-dimethyl-2,6-dioxo-cyclohexylidene)-2-phenyl-ethylamino]-ethylamino}-(toluene-4-sulfonylimino)-methyl]-amino}-ethyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: NH₄PF₆ / CH₂Cl₂; methanol

2: DBU / toluene; CHCl₃ / Heating

With ammonium hexafluorophosphate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In methanol; dichloromethane; chloroform; toluene;
DOI:10.1002/chem.200500876

Reference yield:

: 623929-50-0
[2-(3-{2-[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-2-phenylethylamino]ethyl}thioureido)ethyl]carbamic acid tert-butyl ester

: 879880-71-4
(2-{[{2-[1-(4,4-dimethyl-2,6-dioxo-cyclohexylidene)-2-phenyl-ethylamino]-ethylamino}-(toluene-4-sulfonylimino)-methyl]-amino}-ethyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: acetone

2: NH₄PF₆ / CH₂Cl₂; methanol

3: DBU / toluene; CHCl₃ / Heating

With ammonium hexafluorophosphate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In methanol; dichloromethane; chloroform; acetone; toluene;
DOI:10.1002/chem.200500876