[(3-carbamoyl-4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}phenylcarbamoxy)methyl]carbamic acid benzyl ester

Base Information

Chemical Name:[(3-carbamoyl-4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}phenylcarbamoxy)methyl]carbamic acid benzyl ester
CAS No.:600736-32-1
Molecular Formula:C₂₄H₃₁N₃O₈
Molecular Weight:489.525
Hs Code.:

Synonyms:[(3-carbamoyl-4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}phenylcarbamoxy)methyl]carbamic acid benzyl ester

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Chemical Property of [(3-carbamoyl-4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}phenylcarbamoxy)methyl]carbamic acid benzyl ester

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Technology Process of [(3-carbamoyl-4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}phenylcarbamoxy)methyl]carbamic acid benzyl ester

There total 3 articles about [(3-carbamoyl-4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}phenylcarbamoxy)methyl]carbamic acid benzyl ester 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:

: 600736-31-0
2-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}-5-nitrobenzoylamine

: 600736-32-1
[(3-carbamoyl-4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}phenylcarbamoxy)methyl]carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / Pd/C / methanol / 2 h / 760 Torr

2: 2.59 g / DCC / CH₂Cl₂ / 12 h / 20 °C

With hydrogen; dicyclohexyl-carbodiimide; palladium on activated charcoal; In methanol; dichloromethane;
DOI:10.1021/ja0361897

Reference yield:

: 600736-30-9
2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-5-nitro-benzoic acid

: 600736-32-1
[(3-carbamoyl-4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}phenylcarbamoxy)methyl]carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: trimethylacetyl chloride; Et₃N / CH₂Cl₂ / 1 h / 0 °C

1.2: 92.7 percent / ammonium hydroxide / CH₂Cl₂

2.1: H₂ / Pd/C / methanol / 2 h / 760 Torr

3.1: 2.59 g / DCC / CH₂Cl₂ / 12 h / 20 °C

With hydrogen; pivaloyl chloride; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In methanol; dichloromethane;
DOI:10.1021/ja0361897