N'-<5-<<4-<<5-pentyl>amino>-1,4-dioxobutyl>(phenylmethoxy)amino>pentyl>-N-(5-ethoxy-5-iminopentyl)-N-(phenylmethoxy)butanediamide hydrochloride

Base Information

• Chemical Name: N'-<5-<<4-<<5-pentyl>amino>-1,4-dioxobutyl>(phenylmethoxy)amino>pentyl>-N-(5-ethoxy-5-iminopentyl)-N-(phenylmethoxy)butanediamide hydrochloride
• CAS No.: 123152-39-6
• Molecular Formula: C₄₈H₆₈N₆O₉*ClH
• Molecular Weight: 909.564
• Mol file: 123152-39-6.mol

Synonyms:

Chemical Property of N'-<5-<<4-<<5-pentyl>amino>-1,4-dioxobutyl>(phenylmethoxy)amino>pentyl>-N-(5-ethoxy-5-iminopentyl)-N-(phenylmethoxy)butanediamide hydrochloride

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N'-<5-<<4-<<5-pentyl>amino>-1,4-dioxobutyl>(phenylmethoxy)amino>pentyl>-N-(5-ethoxy-5-iminopentyl)-N-(phenylmethoxy)butanediamide hydrochloride

There total 1 articles about N'-<5-<<4-<<5-pentyl>amino>-1,4-dioxobutyl>(phenylmethoxy)amino>pentyl>-N-(5-ethoxy-5-iminopentyl)-N-(phenylmethoxy)butanediamide hydrochloride 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:

ethanol (64-17-5) + N'-<5-<<4-<<5-pentyl>amino>-1,4-dioxobutyl>(phenylmethoxy)amino>pentyl>-N-(4-cyanobutyl)-N-(phenylmethoxy)butanediamide (112139-65-8) → N'-<5-<<4-<<5-pentyl>amino>-1,4-dioxobutyl>(phenylmethoxy)amino>pentyl>-N-(5-ethoxy-5-iminopentyl)-N-(phenylmethoxy)butanediamide hydrochloride (123152-39-6)

Guidance literature:

With hydrogenchloride; at -20 ℃; for 20h;

DOI:10.1021/jo00284a044

Reference yield:

N'-<5-<<4-<<5-pentyl>amino>-1,4-dioxobutyl>(phenylmethoxy)amino>pentyl>-N-(5-ethoxy-5-iminopentyl)-N-(phenylmethoxy)butanediamide hydrochloride (123152-39-6) → N'-<5-<<4-<<5-pentyl>amino>-1,4-dioxobutyl>(phenylmethoxy)amino>pentyl>-N-(4-(ethoxycarbonyl)butyl)-N-(phenylmethoxy)butanediamide (123152-40-9)

Guidance literature:

With water; at 0 ℃; for 6h; Yield given;

DOI:10.1021/jo00284a044

Reference yield:

N'-<5-<<4-<<5-pentyl>amino>-1,4-dioxobutyl>(phenylmethoxy)amino>pentyl>-N-(5-ethoxy-5-iminopentyl)-N-(phenylmethoxy)butanediamide hydrochloride (123152-39-6) → N'-<5-<<4-<<5-pentyl>amino>-1,4-dioxobutyl>(phenylmethoxy)amino>pentyl>-N-(5-hydroxypentyl)-N-(phenylmethoxy)butanediamide (123152-43-2)

Guidance literature:

Multi-step reaction with 4 steps

1: H₂O / 6 h / 0 °C

2: 55 percent / aq. KOH / acetone / Ambient temperature

3: dicyclohexylcarbodiimide (DCC), (dimethylamino)pyridine / CH₂Cl₂ / Ambient temperature

4: NaBH₄ / ethanol / 2 h / Ambient temperature

With dmap; potassium hydroxide; sodium tetrahydroborate; water; dicyclohexyl-carbodiimide; In ethanol; dichloromethane; acetone;

DOI:10.1021/jo00284a044

upstream raw materials:

ethanol

N'-<5-<<4-<<5-pentyl>amino>-1,4-dioxobutyl>(phenylmethoxy)amino>pentyl>-N-(4-cyanobutyl)-N-(phenylmethoxy)butanediamide

Downstream raw materials:

N'-<5-<<4-<<5-pentyl>amino>-1,4-dioxobutyl>(phenylmethoxy)amino>pentyl>-N-(4-(ethoxycarbonyl)butyl)-N-(phenylmethoxy)butanediamide

N'-<5-<<4-<<5-pentyl>amino>-1,4-dioxobutyl>(phenylmethoxy)amino>pentyl>-N-(5-hydroxypentyl)-N-(phenylmethoxy)butanediamide

N'-<5-<<4-<<5-pentyl>amino>-1,4-dioxobutyl>(phenylmethoxy)amino>pentyl>-N-(4-carboxybutyl)-N-(phenylmethoxy)butanediamide

N'-<5-<<4-<<5-pentyl>amino>-1,4-dioxobutyl>(phenylmethoxy)amino>pentyl>-N-(4-((phenylthio)carbonyl)butyl)-N-(phenylmethoxy)butanediamide