(Z)-N-benzylidene-2-(tert-butoxycarbonylamino)-1-(5-iodo-1H-indol-3-yl)ethanamine N-oxide

Base Information

Chemical Name:(Z)-N-benzylidene-2-(tert-butoxycarbonylamino)-1-(5-iodo-1H-indol-3-yl)ethanamine N-oxide
CAS No.:1309463-79-3
Molecular Formula:C₂₂H₂₄IN₃O₃
Molecular Weight:505.355
Hs Code.:

Synonyms:(Z)-N-benzylidene-2-(tert-butoxycarbonylamino)-1-(5-iodo-1H-indol-3-yl)ethanamine N-oxide

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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 (Z)-N-benzylidene-2-(tert-butoxycarbonylamino)-1-(5-iodo-1H-indol-3-yl)ethanamine N-oxide

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Technology Process of (Z)-N-benzylidene-2-(tert-butoxycarbonylamino)-1-(5-iodo-1H-indol-3-yl)ethanamine N-oxide

There total 4 articles about (Z)-N-benzylidene-2-(tert-butoxycarbonylamino)-1-(5-iodo-1H-indol-3-yl)ethanamine N-oxide 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: 68.0%

: 1309463-63-5
tert-butyl 2-(benzyl(hydroxy)amino)-2-(5-iodo-1H-indol-3-yl)ethylcarbamate

: 1309463-79-3
(Z)-N-benzylidene-2-(tert-butoxycarbonylamino)-1-(5-iodo-1H-indol-3-yl)ethanamine N-oxide

Guidance literature:: With manganese(IV) oxide; In toluene; at 100 ℃; for 0.0833333h;
DOI:10.1016/j.bmc.2011.03.060

Reference yield: 68.0%

: 1309463-79-3
(Z)-N-benzylidene-2-(tert-butoxycarbonylamino)-1-(5-iodo-1H-indol-3-yl)ethanamine N-oxide

Guidance literature:: With manganese(IV) oxide; In toluene; at 100 ℃; for 0.166667h;

Reference yield:

: 16066-91-4
5-iodo-1H-indole

: 1309463-79-3
(Z)-N-benzylidene-2-(tert-butoxycarbonylamino)-1-(5-iodo-1H-indol-3-yl)ethanamine N-oxide

Guidance literature:: Multi-step reaction with 2 steps

1: methanol; acetyl chloride / 2 h / 0 °C

2: manganese(IV) oxide / toluene / 0.08 h / 100 °C

With methanol; manganese(IV) oxide; acetyl chloride; In toluene;
DOI:10.1016/j.bmc.2011.03.060