tert-butyl N-[[(tert-butoxy)carbonyl]amino([(1S)-1-[3-(4-octylphenyl)-1,2,4-oxadiazol-5-yl]ethyl]amino)methylidene]carbamate

Base Information

Chemical Name:tert-butyl N-[[(tert-butoxy)carbonyl]amino([(1S)-1-[3-(4-octylphenyl)-1,2,4-oxadiazol-5-yl]ethyl]amino)methylidene]carbamate
CAS No.:1449767-50-3
Molecular Formula:C₂₉H₄₅N₅O₅
Molecular Weight:543.707
Hs Code.:

Synonyms:tert-butyl N-[[(tert-butoxy)carbonyl]amino([(1S)-1-[3-(4-octylphenyl)-1,2,4-oxadiazol-5-yl]ethyl]amino)methylidene]carbamate

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Chemical Property of tert-butyl N-[[(tert-butoxy)carbonyl]amino([(1S)-1-[3-(4-octylphenyl)-1,2,4-oxadiazol-5-yl]ethyl]amino)methylidene]carbamate

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Technology Process of tert-butyl N-[[(tert-butoxy)carbonyl]amino([(1S)-1-[3-(4-octylphenyl)-1,2,4-oxadiazol-5-yl]ethyl]amino)methylidene]carbamate

There total 7 articles about tert-butyl N-[[(tert-butoxy)carbonyl]amino([(1S)-1-[3-(4-octylphenyl)-1,2,4-oxadiazol-5-yl]ethyl]amino)methylidene]carbamate 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: 81.0%

: 1449767-49-0
(S)-1-(3-(4-octylphenyl)-1,2,4-oxadiazol-5-yl)ethanamine

: 152120-54-2,862686-58-6,1143572-00-2
N,N'-bis( tert-butoxycarbonyl)-1H-pyrazole-1-carboxamidine

: 1449767-50-3
tert-butyl N-[[(tert-butoxy)carbonyl]amino([(1S)-1-[3-(4-octylphenyl)-1,2,4-oxadiazol-5-yl]ethyl]amino)methylidene]carbamate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃; Inert atmosphere;
DOI:10.1021/jm501760d

Reference yield: 81.0%

: 1449767-50-3
tert-butyl N-[[(tert-butoxy)carbonyl]amino([(1S)-1-[3-(4-octylphenyl)-1,2,4-oxadiazol-5-yl]ethyl]amino)methylidene]carbamate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃;

Reference yield:

: 3058-39-7
4-iodobenzonitrile

: 1449767-50-3
tert-butyl N-[[(tert-butoxy)carbonyl]amino([(1S)-1-[3-(4-octylphenyl)-1,2,4-oxadiazol-5-yl]ethyl]amino)methylidene]carbamate

Guidance literature:: Multi-step reaction with 5 steps

1.1: 9-borabicyclo[3.3.1]nonane dimer / tetrahydrofuran / 20 °C / Inert atmosphere

1.2: 18 h / 80 °C / Inert atmosphere

2.1: hydroxylamine hydrochloride; triethylamine / ethanol / 4 h / Inert atmosphere; Reflux

3.1: N-ethyl-N,N-diisopropylamine; 6-chloro-3-((dimethylamino)(dimethyliminio)methyl)-1H-benzo[d][1,2,3]triazol-3-ium-1-olatehexafluorophosphate(V) / N,N-dimethyl-formamide / 18 h / 20 - 80 °C / Inert atmosphere

4.1: trifluoroacetic acid / dichloromethane / 20 °C / Inert atmosphere

5.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 20 °C / Inert atmosphere

With 9-borabicyclo[3.3.1]nonane dimer; 6-chloro-3-((dimethylamino)(dimethyliminio)methyl)-1H-benzo[d][1,2,3]triazol-3-ium-1-olatehexafluorophosphate(V); hydroxylamine hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile; 1.2: |Suzuki-Miyaura Coupling;
DOI:10.1021/jm501760d