2,2,2-trifluoro-N-[3-(6-{8-[6-(5-iodo-2-methoxybenzylamino)hexylamino]octylamino}hexylamino)propyl]acetamide

Base Information

Chemical Name:2,2,2-trifluoro-N-[3-(6-{8-[6-(5-iodo-2-methoxybenzylamino)hexylamino]octylamino}hexylamino)propyl]acetamide
CAS No.:428880-35-7
Molecular Formula:C₃₃H₅₉F₃IN₅O₂
Molecular Weight:741.763
Hs Code.:

Synonyms:2,2,2-trifluoro-N-[3-(6-{8-[6-(5-iodo-2-methoxybenzylamino)hexylamino]octylamino}hexylamino)propyl]acetamide

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Chemical Property of 2,2,2-trifluoro-N-[3-(6-{8-[6-(5-iodo-2-methoxybenzylamino)hexylamino]octylamino}hexylamino)propyl]acetamide

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Technology Process of 2,2,2-trifluoro-N-[3-(6-{8-[6-(5-iodo-2-methoxybenzylamino)hexylamino]octylamino}hexylamino)propyl]acetamide

There total 6 articles about 2,2,2-trifluoro-N-[3-(6-{8-[6-(5-iodo-2-methoxybenzylamino)hexylamino]octylamino}hexylamino)propyl]acetamide 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:

: 2,2,2-Trifluoro-N-(3-{6-[8-(6-{[1-(5-iodo-2-methoxy-phenyl)-meth-(Z)-ylidene]-amino}-hexylamino)-octylamino]-hexylamino}-propyl)-acetamide

: 428880-35-7
2,2,2-trifluoro-N-[3-(6-{8-[6-(5-iodo-2-methoxybenzylamino)hexylamino]octylamino}hexylamino)propyl]acetamide

Guidance literature:: With sodium tetrahydroborate; In ethanol; at 0 ℃; for 4h;
DOI:10.1021/jm011067f

Reference yield:

: 428880-31-3
{8-[tert-butoxycarbonyl-(6-tert-butoxycarbonylaminohexyl)amino]octyl}-{6-[tert-butoxycarbonyl-(2-cyanoethyl)amino]hexyl}carbamic acid tert-butyl ester

: 428880-35-7
2,2,2-trifluoro-N-[3-(6-{8-[6-(5-iodo-2-methoxybenzylamino)hexylamino]octylamino}hexylamino)propyl]acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: 90 percent / H₂; 40percent aq. NaOH / Raney Ni / ethanol / 6 h / 20 °C / 775.74 Torr

2: 90 percent / methanol / 2 h / -80 - 0 °C

3: 56 percent / CF₃COOH / CH₂Cl₂ / 2 h / 20 °C

4: toluene / 5 h / Heating

5: NaBH₄ / ethanol / 4 h / 0 °C

With sodium tetrahydroborate; hydrogen; trifluoroacetic acid; nickel; In methanol; ethanol; dichloromethane; toluene;
DOI:10.1021/jm011067f

Reference yield:

: 428879-87-2
{8-[(6-aminohexyl)-tert-butoxycarbonylamino]octyl}-(6-tert-butoxycarbonylaminohexyl)carbamic acid tert-butyl ester

: 428880-35-7
2,2,2-trifluoro-N-[3-(6-{8-[6-(5-iodo-2-methoxybenzylamino)hexylamino]octylamino}hexylamino)propyl]acetamide

Guidance literature:: Multi-step reaction with 6 steps

1: 70 percent / methanol / 20 °C

2: 90 percent / H₂; 40percent aq. NaOH / Raney Ni / ethanol / 6 h / 20 °C / 775.74 Torr

3: 90 percent / methanol / 2 h / -80 - 0 °C

4: 56 percent / CF₃COOH / CH₂Cl₂ / 2 h / 20 °C

5: toluene / 5 h / Heating

6: NaBH₄ / ethanol / 4 h / 0 °C

With sodium tetrahydroborate; hydrogen; trifluoroacetic acid; nickel; In methanol; ethanol; dichloromethane; toluene;
DOI:10.1021/jm011067f