N-(3-{benzyl[4-(4-(2-carboxyethyl)phenoxy)benzyl]amino}-2-methylphenyl)methanesulfonamide

Base Information

Chemical Name:N-(3-{benzyl[4-(4-(2-carboxyethyl)phenoxy)benzyl]amino}-2-methylphenyl)methanesulfonamide
CAS No.:448957-04-8
Molecular Formula:C₃₁H₃₂N₂O₅S
Molecular Weight:544.671
Hs Code.:

Synonyms:N-(3-{benzyl[4-(4-(2-carboxyethyl)phenoxy)benzyl]amino}-2-methylphenyl)methanesulfonamide

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Chemical Property of N-(3-{benzyl[4-(4-(2-carboxyethyl)phenoxy)benzyl]amino}-2-methylphenyl)methanesulfonamide

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Technology Process of N-(3-{benzyl[4-(4-(2-carboxyethyl)phenoxy)benzyl]amino}-2-methylphenyl)methanesulfonamide

There total 7 articles about N-(3-{benzyl[4-(4-(2-carboxyethyl)phenoxy)benzyl]amino}-2-methylphenyl)methanesulfonamide 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%

: 3-[4-(4-{[benzyl-(3-methanesulfonylamino-2-methyl-phenyl)-amino]-methyl}-phenoxy)-phenyl]-propionic acid ethyl ester

: 448957-04-8
N-(3-{benzyl[4-(4-(2-carboxyethyl)phenoxy)benzyl]amino}-2-methylphenyl)methanesulfonamide

Guidance literature:: With sodium hydroxide; In tetrahydrofuran; ethanol; at 20 ℃; for 12h;
DOI:10.1016/j.bmcl.2004.06.022

Reference yield:

: 106-41-2
4-bromo-phenol

: 448957-04-8
N-(3-{benzyl[4-(4-(2-carboxyethyl)phenoxy)benzyl]amino}-2-methylphenyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 8 steps

1: 79 percent / K₂CO₃ / dimethylformamide / 12 h / 100 °C

2: AcOH / 1,2-dichloro-ethane / 4 h / 20 °C

3: Na(OAc)3BH / 1,2-dichloro-ethane / 12 h

4: 87 percent / i-Pr₂NEt / dimethylformamide / 12 h / 95 °C

5: Fe; NH₄Cl / 1 h / 80 °C

6: pyridine / 1 h / 20 °C

7: 77 percent / Pd(PPh₃)4 / tetrahydrofuran / 12 h / 75 °C

8: 98 percent / aq. NaOH / tetrahydrofuran; ethanol / 12 h / 20 °C

With pyridine; sodium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium tris(acetoxy)borohydride; iron; potassium carbonate; ammonium chloride; acetic acid; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2004.06.022

Reference yield:

: 459-57-4
4-fluorobenzaldehyde

: 448957-04-8
N-(3-{benzyl[4-(4-(2-carboxyethyl)phenoxy)benzyl]amino}-2-methylphenyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 8 steps

1: 79 percent / K₂CO₃ / dimethylformamide / 12 h / 100 °C

2: AcOH / 1,2-dichloro-ethane / 4 h / 20 °C

3: Na(OAc)3BH / 1,2-dichloro-ethane / 12 h

4: 87 percent / i-Pr₂NEt / dimethylformamide / 12 h / 95 °C

5: Fe; NH₄Cl / 1 h / 80 °C

6: pyridine / 1 h / 20 °C

7: 77 percent / Pd(PPh₃)4 / tetrahydrofuran / 12 h / 75 °C

8: 98 percent / aq. NaOH / tetrahydrofuran; ethanol / 12 h / 20 °C

With pyridine; sodium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium tris(acetoxy)borohydride; iron; potassium carbonate; ammonium chloride; acetic acid; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2004.06.022