N-(2,4-dimethoxy-benzyloxy)-3-(4-phenoxy-phenylsulfamoyl)-N-(2,4,6-trimethoxy-benzyl)-propionamide

Base Information

Chemical Name:N-(2,4-dimethoxy-benzyloxy)-3-(4-phenoxy-phenylsulfamoyl)-N-(2,4,6-trimethoxy-benzyl)-propionamide
CAS No.:216067-75-3
Molecular Formula:C₃₄H₃₈N₂O₁₀S
Molecular Weight:666.749
Hs Code.:

<i>N</i>-(2,4-dimethoxy-benzyloxy)-3-(4-phenoxy-phenylsulfamoyl)-<i>N</i>-(2,4,6-trimethoxy-benzyl)-propionamide

Synonyms:N-(2,4-dimethoxy-benzyloxy)-3-(4-phenoxy-phenylsulfamoyl)-N-(2,4,6-trimethoxy-benzyl)-propionamide

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Chemical Property of N-(2,4-dimethoxy-benzyloxy)-3-(4-phenoxy-phenylsulfamoyl)-N-(2,4,6-trimethoxy-benzyl)-propionamide

Chemical Property:

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Technology Process of N-(2,4-dimethoxy-benzyloxy)-3-(4-phenoxy-phenylsulfamoyl)-N-(2,4,6-trimethoxy-benzyl)-propionamide

There total 6 articles about N-(2,4-dimethoxy-benzyloxy)-3-(4-phenoxy-phenylsulfamoyl)-N-(2,4,6-trimethoxy-benzyl)-propionamide 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:

: 7314-44-5
2,4-dimethoxylbenzyl alcohol

: 216067-75-3
N-(2,4-dimethoxy-benzyloxy)-3-(4-phenoxy-phenylsulfamoyl)-N-(2,4,6-trimethoxy-benzyl)-propionamide

Guidance literature:: Multi-step reaction with 6 steps

1: 82 percent / triphenylphosphine, diethylazodicarboxylate / CHCl₃ / Ambient temperature

2: 95 percent / hydrazine hydrate / ethanol / 0.25 h / Heating

3: 92 percent / CH₂Cl₂ / 4 h

4: 85 percent / NaBH₃CN / ethanol; aq. HCl / 1 h / pH=3

5: diisopropylethylamine / CH₂Cl₂ / 0.25 h / -78 °C

6: CH₂Cl₂

With sodium cyanoborohydride; hydrazine hydrate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; diethylazodicarboxylate; In hydrogenchloride; ethanol; dichloromethane; chloroform;
DOI:10.1016/S0040-4039(98)01760-2

Reference yield:

: 216067-66-2
O-(2,4-dimethoxy-benzyl)-hydroxylamine

: 216067-75-3
N-(2,4-dimethoxy-benzyloxy)-3-(4-phenoxy-phenylsulfamoyl)-N-(2,4,6-trimethoxy-benzyl)-propionamide

Guidance literature:: Multi-step reaction with 4 steps

1: 92 percent / CH₂Cl₂ / 4 h

2: 85 percent / NaBH₃CN / ethanol; aq. HCl / 1 h / pH=3

3: diisopropylethylamine / CH₂Cl₂ / 0.25 h / -78 °C

4: CH₂Cl₂

With sodium cyanoborohydride; N-ethyl-N,N-diisopropylamine; In hydrogenchloride; ethanol; dichloromethane;
DOI:10.1016/S0040-4039(98)01760-2

Reference yield:

: 216067-79-7
N-[(2,4-Dimethoxyphenyl)methyl]phthalimide

: 216067-75-3
N-(2,4-dimethoxy-benzyloxy)-3-(4-phenoxy-phenylsulfamoyl)-N-(2,4,6-trimethoxy-benzyl)-propionamide

Guidance literature:: Multi-step reaction with 5 steps

1: 95 percent / hydrazine hydrate / ethanol / 0.25 h / Heating

2: 92 percent / CH₂Cl₂ / 4 h

3: 85 percent / NaBH₃CN / ethanol; aq. HCl / 1 h / pH=3

4: diisopropylethylamine / CH₂Cl₂ / 0.25 h / -78 °C

5: CH₂Cl₂

With sodium cyanoborohydride; hydrazine hydrate; N-ethyl-N,N-diisopropylamine; In hydrogenchloride; ethanol; dichloromethane;
DOI:10.1016/S0040-4039(98)01760-2