5-((((5-hydroxycarbonyl-2,4-dioctyloxy)phenylcarbonyl)aminomethylcarbonyl)ammino)-2-octyloxy-N-hexylbenzamide

Base Information

Chemical Name:5-((((5-hydroxycarbonyl-2,4-dioctyloxy)phenylcarbonyl)aminomethylcarbonyl)ammino)-2-octyloxy-N-hexylbenzamide
CAS No.:416899-35-9
Molecular Formula:C₄₇H₇₅N₃O₈
Molecular Weight:810.128
Hs Code.:

Synonyms:5-((((5-hydroxycarbonyl-2,4-dioctyloxy)phenylcarbonyl)aminomethylcarbonyl)ammino)-2-octyloxy-N-hexylbenzamide

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Chemical Property of 5-((((5-hydroxycarbonyl-2,4-dioctyloxy)phenylcarbonyl)aminomethylcarbonyl)ammino)-2-octyloxy-N-hexylbenzamide

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Technology Process of 5-((((5-hydroxycarbonyl-2,4-dioctyloxy)phenylcarbonyl)aminomethylcarbonyl)ammino)-2-octyloxy-N-hexylbenzamide

There total 14 articles about 5-((((5-hydroxycarbonyl-2,4-dioctyloxy)phenylcarbonyl)aminomethylcarbonyl)ammino)-2-octyloxy-N-hexylbenzamide 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: 98.0%

: 416899-34-8
5-((((5-methoxycarbonyl-2,4-dioctyloxy)phenylcarbonyl)aminomethylcarbonyl)amino)-2-octyloxy-N-hexylbenzamide

: 416899-35-9
5-((((5-hydroxycarbonyl-2,4-dioctyloxy)phenylcarbonyl)aminomethylcarbonyl)ammino)-2-octyloxy-N-hexylbenzamide

Guidance literature:: With potassium hydroxide; In dimethyl sulfoxide; for 0.333333h; Heating;
DOI:10.1021/ja010701b

Reference yield:

: 416899-32-6
5-(((phenylmethoxy)carbonyl)aminomethylcarbonylamino)-2-octyloxy-N-hexylbenzamide

: 416899-35-9
5-((((5-hydroxycarbonyl-2,4-dioctyloxy)phenylcarbonyl)aminomethylcarbonyl)ammino)-2-octyloxy-N-hexylbenzamide

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / hydrogen / Pd-C / methanol; dimethylformamide / 30 - 40 °C

2: 52 percent / EDC; HOBT / CH₂Cl₂ / Heating

3: 98 percent / aq. KOH / dimethylsulfoxide / 0.33 h / Heating

With potassium hydroxide; hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; palladium on activated charcoal; In methanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1021/ja010701b

Reference yield:

: 267897-53-0
N-hexyl-5-amino-2-(octyloxy)benzamide

: 416899-35-9
5-((((5-hydroxycarbonyl-2,4-dioctyloxy)phenylcarbonyl)aminomethylcarbonyl)ammino)-2-octyloxy-N-hexylbenzamide

Guidance literature:: Multi-step reaction with 4 steps

1: 64 percent / EDC; HOBT / CH₂Cl₂

2: 96 percent / hydrogen / Pd-C / methanol; dimethylformamide / 30 - 40 °C

3: 52 percent / EDC; HOBT / CH₂Cl₂ / Heating

4: 98 percent / aq. KOH / dimethylsulfoxide / 0.33 h / Heating

With potassium hydroxide; hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; palladium on activated charcoal; In methanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1021/ja010701b