N,N'-(3,7,13,17-tetrathioxo-4,8,12,16-tetraazanonadecane-1,19-diyl)bis(4-cyclohexyloxybenzamide)

Base Information

Chemical Name:N,N'-(3,7,13,17-tetrathioxo-4,8,12,16-tetraazanonadecane-1,19-diyl)bis(4-cyclohexyloxybenzamide)
CAS No.:1280551-82-7
Molecular Formula:C₄₁H₅₈N₆O₂S₆
Molecular Weight:859.347
Hs Code.:

Synonyms:N,N'-(3,7,13,17-tetrathioxo-4,8,12,16-tetraazanonadecane-1,19-diyl)bis(4-cyclohexyloxybenzamide)

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Chemical Property of N,N'-(3,7,13,17-tetrathioxo-4,8,12,16-tetraazanonadecane-1,19-diyl)bis(4-cyclohexyloxybenzamide)

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Technology Process of N,N'-(3,7,13,17-tetrathioxo-4,8,12,16-tetraazanonadecane-1,19-diyl)bis(4-cyclohexyloxybenzamide)

There total 8 articles about N,N'-(3,7,13,17-tetrathioxo-4,8,12,16-tetraazanonadecane-1,19-diyl)bis(4-cyclohexyloxybenzamide) 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: 96.0%

: 1280551-86-1
N,N'-(3,7,13,17-tetraoxo-4,8,12,16-tetraazanonadecane-1,19-diyl)bis(4-cyclohexyloxybenzamide)

: 1280551-82-7
N,N'-(3,7,13,17-tetrathioxo-4,8,12,16-tetraazanonadecane-1,19-diyl)bis(4-cyclohexyloxybenzamide)

Guidance literature:: With Lawessons reagent; In pyridine; at 100 ℃; for 23h; Inert atmosphere;
DOI:10.1002/ejoc.201001695

Reference yield: 96.0%

: 1280551-82-7
N,N'-(3,7,13,17-tetrathioxo-4,8,12,16-tetraazanonadecane-1,19-diyl)bis(4-cyclohexyloxybenzamide)

Guidance literature:

Reference yield:

: 1280551-88-3
benzyl 3-(4-cyclohexyloxybenzamido)propanoate

: 1280551-82-7
N,N'-(3,7,13,17-tetrathioxo-4,8,12,16-tetraazanonadecane-1,19-diyl)bis(4-cyclohexyloxybenzamide)

Guidance literature:: Multi-step reaction with 3 steps

1.1: palladium 10% on activated carbon; hydrogen / methanol / 3.5 h / 20 °C

2.1: hydrogenchloride / 1,4-dioxane; methanol / 3 h / 50 °C / Inert atmosphere; Sonication

2.2: 68 h / 30 °C / Inert atmosphere

3.1: Lawessons reagent / pyridine / 23 h / 100 °C / Inert atmosphere

With Lawessons reagent; hydrogenchloride; palladium 10% on activated carbon; hydrogen; In 1,4-dioxane; pyridine; methanol;
DOI:10.1002/ejoc.201001695