N-[1-{[Acetyl-(3-methoxy-benzyl)-amino]-methyl}-2-(1H-indol-3-yl)-ethyl]-2-bromo-acetamide

Base Information

Chemical Name:N-[1-{[Acetyl-(3-methoxy-benzyl)-amino]-methyl}-2-(1H-indol-3-yl)-ethyl]-2-bromo-acetamide
CAS No.:1027378-35-3
Molecular Formula:C₂₃H₂₆BrN₃O₃
Molecular Weight:472.382
Hs Code.:

Synonyms:N-[1-{[Acetyl-(3-methoxy-benzyl)-amino]-methyl}-2-(1H-indol-3-yl)-ethyl]-2-bromo-acetamide

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Chemical Property of N-[1-{[Acetyl-(3-methoxy-benzyl)-amino]-methyl}-2-(1H-indol-3-yl)-ethyl]-2-bromo-acetamide

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Technology Process of N-[1-{[Acetyl-(3-methoxy-benzyl)-amino]-methyl}-2-(1H-indol-3-yl)-ethyl]-2-bromo-acetamide

There total 7 articles about N-[1-{[Acetyl-(3-methoxy-benzyl)-amino]-methyl}-2-(1H-indol-3-yl)-ethyl]-2-bromo-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:

: 598-21-0
2-Bromoacetyl bromide

: 1025921-49-6
N-[2-Amino-3-(1H-indol-3-yl)-propyl]-N-(3-methoxy-benzyl)-acetamide

: 1027378-35-3
N-[1-{[Acetyl-(3-methoxy-benzyl)-amino]-methyl}-2-(1H-indol-3-yl)-ethyl]-2-bromo-acetamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 0 - 20 ℃; for 2h;
DOI:10.1021/jm950616c

Reference yield:

: 170568-17-9
(RS)-1-amino-3-(1H-indol-3-yl)-2-(N-(triphenylmethyl)amino)propane

: 1027378-35-3
N-[1-{[Acetyl-(3-methoxy-benzyl)-amino]-methyl}-2-(1H-indol-3-yl)-ethyl]-2-bromo-acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: toluene

2: sodium borohydride / tetrahydrofuran; methanol / 4 h

3: triethylamine / tetrahydrofuran / 4 h / 0 °C

4: formic acid / CH₂Cl₂ / 4 h / 0 - 20 °C

5: diisopropylethylamine / tetrahydrofuran / 2 h / 0 - 20 °C

With sodium tetrahydroborate; formic acid; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; toluene;
DOI:10.1021/jm950616c

Reference yield:

: 170568-16-8
(RS)-3-(1H-indol-3-yl)-2-(N-(triphenylmethyl)amino)propanamide

: 1027378-35-3
N-[1-{[Acetyl-(3-methoxy-benzyl)-amino]-methyl}-2-(1H-indol-3-yl)-ethyl]-2-bromo-acetamide

Guidance literature:: Multi-step reaction with 6 steps

1: 48.68 g / borane methyl sulfide complex / tetrahydrofuran / 83 °C

2: toluene

3: sodium borohydride / tetrahydrofuran; methanol / 4 h

4: triethylamine / tetrahydrofuran / 4 h / 0 °C

5: formic acid / CH₂Cl₂ / 4 h / 0 - 20 °C

6: diisopropylethylamine / tetrahydrofuran / 2 h / 0 - 20 °C

With sodium tetrahydroborate; formic acid; dimethylsulfide borane complex; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; toluene;
DOI:10.1021/jm950616c