{1-(1H-indol-3-ylmethyl)-2-[5-(3-phenyl-1H-indazol-5-yl)-pyridin-3-yloxy]-ethyl}-carbamic acid tert-butyl ester

Base Information

Chemical Name:{1-(1H-indol-3-ylmethyl)-2-[5-(3-phenyl-1H-indazol-5-yl)-pyridin-3-yloxy]-ethyl}-carbamic acid tert-butyl ester
CAS No.:911305-68-5
Molecular Formula:C₃₄H₃₃N₅O₃
Molecular Weight:559.668
Hs Code.:

{1-(1<i>H</i>-indol-3-ylmethyl)-2-[5-(3-phenyl-1<i>H</i>-indazol-5-yl)-pyridin-3-yloxy]-ethyl}-carbamic acid <i>tert</i>-butyl ester

Synonyms:{1-(1H-indol-3-ylmethyl)-2-[5-(3-phenyl-1H-indazol-5-yl)-pyridin-3-yloxy]-ethyl}-carbamic acid tert-butyl ester

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of {1-(1H-indol-3-ylmethyl)-2-[5-(3-phenyl-1H-indazol-5-yl)-pyridin-3-yloxy]-ethyl}-carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of {1-(1H-indol-3-ylmethyl)-2-[5-(3-phenyl-1H-indazol-5-yl)-pyridin-3-yloxy]-ethyl}-carbamic acid tert-butyl ester

There total 5 articles about {1-(1H-indol-3-ylmethyl)-2-[5-(3-phenyl-1H-indazol-5-yl)-pyridin-3-yloxy]-ethyl}-carbamic acid tert-butyl 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:

: 900517-08-0
(S)-[1-(1H-indol-3-ylmethyl)-2-(5-trimethylstannylpyridin-3-yloxy)ethyl]carbamic acid tert-butyl ester

: 57639-16-4
5-Bromo-3-phenylindazole

: 911305-68-5
{1-(1H-indol-3-ylmethyl)-2-[5-(3-phenyl-1H-indazol-5-yl)-pyridin-3-yloxy]-ethyl}-carbamic acid tert-butyl ester

Guidance literature:: With triethylamine; tris-(o-tolyl)phosphine; palladium bis(dibenzylideneacetone)palladium⁽⁰⁾; In N,N-dimethyl-formamide; at 110 ℃; for 4h;
DOI:10.1016/j.bmc.2006.06.047

Reference yield:

: 885124-18-5
(5-bromo-2-fluorophenyl)-phenyl-methanol

: 911305-68-5
{1-(1H-indol-3-ylmethyl)-2-[5-(3-phenyl-1H-indazol-5-yl)-pyridin-3-yloxy]-ethyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: manganese(IV) oxide / dioxane / 4 h / Heating

2: hydrazine monohydrate / 9 h / Heating

3: tri-o-tolylphosphine; triethylamine / Pd₂(dba)2 / dimethylformamide / 4 h / 110 °C

With manganese(IV) oxide; hydrazine hydrate; triethylamine; tris-(o-tolyl)phosphine; palladium bis(dibenzylideneacetone)palladium⁽⁰⁾; In 1,4-dioxane; N,N-dimethyl-formamide; 3: Stille coupling;
DOI:10.1016/j.bmc.2006.06.047

Reference yield:

: 885124-16-3
5-bromo-2-fluorobenzophenone

: 911305-68-5
{1-(1H-indol-3-ylmethyl)-2-[5-(3-phenyl-1H-indazol-5-yl)-pyridin-3-yloxy]-ethyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: hydrazine monohydrate / 9 h / Heating

2: tri-o-tolylphosphine; triethylamine / Pd₂(dba)2 / dimethylformamide / 4 h / 110 °C

With hydrazine hydrate; triethylamine; tris-(o-tolyl)phosphine; palladium bis(dibenzylideneacetone)palladium⁽⁰⁾; In N,N-dimethyl-formamide; 2: Stille coupling;
DOI:10.1016/j.bmc.2006.06.047