1-[p-(N,N-Diethylamino)phenyl]-4(S)-hydroxy-5(S)-2,5-bis[N-(N-methoxycarbonyl-(L)-tert-leucyl)amino]-6-phenyl-2-azahexane

Base Information

Chemical Name:1-[p-(N,N-Diethylamino)phenyl]-4(S)-hydroxy-5(S)-2,5-bis[N-(N-methoxycarbonyl-(L)-tert-leucyl)amino]-6-phenyl-2-azahexane
CAS No.:202586-00-3
Molecular Formula:C₃₇H₅₈N₆O₇
Molecular Weight:698.904
Hs Code.:

Synonyms:1-[p-(N,N-Diethylamino)phenyl]-4(S)-hydroxy-5(S)-2,5-bis[N-(N-methoxycarbonyl-(L)-tert-leucyl)amino]-6-phenyl-2-azahexane

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Chemical Property of 1-[p-(N,N-Diethylamino)phenyl]-4(S)-hydroxy-5(S)-2,5-bis[N-(N-methoxycarbonyl-(L)-tert-leucyl)amino]-6-phenyl-2-azahexane

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Technology Process of 1-[p-(N,N-Diethylamino)phenyl]-4(S)-hydroxy-5(S)-2,5-bis[N-(N-methoxycarbonyl-(L)-tert-leucyl)amino]-6-phenyl-2-azahexane

There total 7 articles about 1-[p-(N,N-Diethylamino)phenyl]-4(S)-hydroxy-5(S)-2,5-bis[N-(N-methoxycarbonyl-(L)-tert-leucyl)amino]-6-phenyl-2-azahexane 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:

: 120-21-8
4-Diethylaminobenzaldehyde

: 202586-00-3
1-[p-(N,N-Diethylamino)phenyl]-4(S)-hydroxy-5(S)-2,5-bis[N-(N-methoxycarbonyl-(L)-tert-leucyl)amino]-6-phenyl-2-azahexane

Guidance literature:: Multi-step reaction with 6 steps

1: 91 percent / ethanol / 4 h / Heating

2: 89 percent / H₂ / 10percent Pd/C / methanol

3: 55 percent / propan-2-ol / 16 h / 80 °C

4: 90 percent / aq. K₂CO₃ / methanol / 3 h / Heating

5: 100 percent / 4N HCl / dimethylformamide; dioxane / 4 h / Ambient temperature

6: 1.) O-(1,2-dihydro-2-oxo-1-pyridyl)-N,N,N',N'-tetramethyluronium tetrafluoroborate, N-ethyldiisopropylamine / 1.) DMF, 0 deg C, 20 min, 2.) DMF, overnight

With hydrogenchloride; hydrogen; potassium carbonate; O-(1,2-dihydro-2-oxo-1-pyridyl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In 1,4-dioxane; methanol; ethanol; N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1021/jm970873c

Reference yield:

: N'-[1-(4-Diethylamino-phenyl)-meth-(E)-ylidene]-hydrazinecarboxylic acid tert-butyl ester

: 202586-00-3
1-[p-(N,N-Diethylamino)phenyl]-4(S)-hydroxy-5(S)-2,5-bis[N-(N-methoxycarbonyl-(L)-tert-leucyl)amino]-6-phenyl-2-azahexane

Guidance literature:: Multi-step reaction with 5 steps

1: 89 percent / H₂ / 10percent Pd/C / methanol

2: 55 percent / propan-2-ol / 16 h / 80 °C

3: 90 percent / aq. K₂CO₃ / methanol / 3 h / Heating

4: 100 percent / 4N HCl / dimethylformamide; dioxane / 4 h / Ambient temperature

5: 1.) O-(1,2-dihydro-2-oxo-1-pyridyl)-N,N,N',N'-tetramethyluronium tetrafluoroborate, N-ethyldiisopropylamine / 1.) DMF, 0 deg C, 20 min, 2.) DMF, overnight

With hydrogenchloride; hydrogen; potassium carbonate; O-(1,2-dihydro-2-oxo-1-pyridyl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In 1,4-dioxane; methanol; N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1021/jm970873c