1-{2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl}-3-hexyl-urea

Base Information

Chemical Name:1-{2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl}-3-hexyl-urea
CAS No.:301646-76-4
Molecular Formula:C₅₂H₆₉N₃O₅
Molecular Weight:816.137
Hs Code.:

1-{2-[3,5-bis-(3,5-di-<i>tert</i>-butyl-benzyloxy)-benzyl]-1,3-dioxo-2,3-dihydro-1<i>H</i>-isoindol-5-yl}-3-hexyl-urea

Synonyms:1-{2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl}-3-hexyl-urea

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Chemical Property of 1-{2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl}-3-hexyl-urea

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Technology Process of 1-{2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl}-3-hexyl-urea

There total 4 articles about 1-{2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl}-3-hexyl-urea 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: 50.0%

: 111-26-2
hexan-1-amine

: 32315-10-9
bis(trichloromethyl) carbonate

: 5-amino-2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-isoindole-1,3-dione

: 301646-76-4
1-{2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl}-3-hexyl-urea

Guidance literature:: With triethylamine; In dichloromethane;
DOI:10.1021/ol006157d

Reference yield:

: 89-40-7
4-nitrophthalimide

: 301646-76-4
1-{2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl}-3-hexyl-urea

Guidance literature:: Multi-step reaction with 3 steps

1: 63 percent / K₂CO₃ / acetonitrile

2: 75 percent / H₂ / Raney Ni / ethanol

3: 50 percent / Et₃N / CH₂Cl₂

With hydrogen; potassium carbonate; triethylamine; nickel; In ethanol; dichloromethane; acetonitrile; 1: Substitution / 2: Catalytic hydrogenation / 3: Condensation;
DOI:10.1021/ol006157d

Reference yield:

: 213680-85-4
1,3-bis{[3,5-bis(tert-butyl)benzyl]oxy}-5-(bromomethyl)benzene

: 301646-76-4
1-{2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl}-3-hexyl-urea

Guidance literature:: Multi-step reaction with 3 steps

1: 63 percent / K₂CO₃ / acetonitrile

2: 75 percent / H₂ / Raney Ni / ethanol

3: 50 percent / Et₃N / CH₂Cl₂

With hydrogen; potassium carbonate; triethylamine; nickel; In ethanol; dichloromethane; acetonitrile; 1: Substitution / 2: Catalytic hydrogenation / 3: Condensation;
DOI:10.1021/ol006157d