N-methyl-N-(2-methylphenyl)-2-{3-[N-(2-aminoacetyl)-N-(N-methyl-N-phenylcarbamoylmethyl)amino]phenoxy}acetamide

Base Information

Chemical Name:N-methyl-N-(2-methylphenyl)-2-{3-[N-(2-aminoacetyl)-N-(N-methyl-N-phenylcarbamoylmethyl)amino]phenoxy}acetamide
CAS No.:183180-27-0
Molecular Formula:C₂₇H₃₀N₄O₄
Molecular Weight:474.56
Hs Code.:

Synonyms:N-methyl-N-(2-methylphenyl)-2-{3-[N-(2-aminoacetyl)-N-(N-methyl-N-phenylcarbamoylmethyl)amino]phenoxy}acetamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-methyl-N-(2-methylphenyl)-2-{3-[N-(2-aminoacetyl)-N-(N-methyl-N-phenylcarbamoylmethyl)amino]phenoxy}acetamide

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Technology Process of N-methyl-N-(2-methylphenyl)-2-{3-[N-(2-aminoacetyl)-N-(N-methyl-N-phenylcarbamoylmethyl)amino]phenoxy}acetamide

There total 7 articles about N-methyl-N-(2-methylphenyl)-2-{3-[N-(2-aminoacetyl)-N-(N-methyl-N-phenylcarbamoylmethyl)amino]phenoxy}acetamide 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: 100.0%

: 183180-28-1
N-methyl-N-(2-methylphenyl)-2-(3-{N-[2-(N-tert-butoxycarbonylamino)acetyl]-N-(N-methyl-N-phenylcarbamoylmethyl)amino}phenoxy)acetamide

: 183180-27-0
N-methyl-N-(2-methylphenyl)-2-{3-[N-(2-aminoacetyl)-N-(N-methyl-N-phenylcarbamoylmethyl)amino]phenoxy}acetamide

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 0 ℃; for 1h;
DOI:10.1248/cpb.46.951

Reference yield:

: 1484-26-0
3-(benzyloxy)aniline

: 183180-27-0
N-methyl-N-(2-methylphenyl)-2-{3-[N-(2-aminoacetyl)-N-(N-methyl-N-phenylcarbamoylmethyl)amino]phenoxy}acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: 68 percent / EDC*HCl, DMAP / CH₂Cl₂ / 12 h / Ambient temperature

2: 1.) NaH / 1.) THF, 55 deg C, 20 min, 2.) THF, RT, 1.5 h

3: 82 percent / H₂ / 5percent Pd/C / ethanol / 2 h / 760 Torr

4: 99 percent / K₂CO₃ / dimethylformamide / 70 °C

5: 100 percent / TFA / CH₂Cl₂ / 1 h / 0 °C

With dmap; hydrogen; sodium hydride; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; palladium on activated charcoal; In ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1248/cpb.46.951

Reference yield:

: 212116-83-1
N-(3-benzyloxyphenyl)-2-(N-tert-butoxycarbonylamino)acetamide

: 183180-27-0
N-methyl-N-(2-methylphenyl)-2-{3-[N-(2-aminoacetyl)-N-(N-methyl-N-phenylcarbamoylmethyl)amino]phenoxy}acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) NaH / 1.) THF, 55 deg C, 20 min, 2.) THF, RT, 1.5 h

2: 82 percent / H₂ / 5percent Pd/C / ethanol / 2 h / 760 Torr

3: 99 percent / K₂CO₃ / dimethylformamide / 70 °C

4: 100 percent / TFA / CH₂Cl₂ / 1 h / 0 °C

With hydrogen; sodium hydride; potassium carbonate; trifluoroacetic acid; palladium on activated charcoal; In ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1248/cpb.46.951