dimethyl 2-((4-chlorophenyl)(methyl)amino)-1H-indole-3,5-dicarboxylate

Base Information

• Chemical Name: dimethyl 2-((4-chlorophenyl)(methyl)amino)-1H-indole-3,5-dicarboxylate
• CAS No.: 1421349-49-6
• Molecular Formula: C₁₉H₁₇ClN₂O₄
• Molecular Weight: 372.808
• Mol file: 1421349-49-6.mol

Synonyms:dimethyl 2-((4-chlorophenyl)(methyl)amino)-1H-indole-3,5-dicarboxylate

Chemical Property of dimethyl 2-((4-chlorophenyl)(methyl)amino)-1H-indole-3,5-dicarboxylate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of dimethyl 2-((4-chlorophenyl)(methyl)amino)-1H-indole-3,5-dicarboxylate

There total 2 articles about dimethyl 2-((4-chlorophenyl)(methyl)amino)-1H-indole-3,5-dicarboxylate 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:

dimethyl 1H-indole-3,5-dicarboxylate (888319-94-6) + N-methyl(p-chloroaniline) (932-96-7) → dimethyl 2-((4-chlorophenyl)(methyl)amino)-1H-indole-3,5-dicarboxylate (1421349-49-6)

Guidance literature:

dimethyl 1H-indole-3,5-dicarboxylate; With N,N'-dimethylpiperazine; N-chloro-succinimide; In dichloromethane; at 0 ℃; Inert atmosphere;

N-methyl(p-chloroaniline); With trichloroacetic acid; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;

DOI:10.1016/j.ejmech.2013.03.072

Reference yield:

5-methoxycarbonylindole (1011-65-0) → dimethyl 2-((4-chlorophenyl)(methyl)amino)-1H-indole-3,5-dicarboxylate (1421349-49-6)

Guidance literature:

Multi-step reaction with 2 steps

1.1: pyridine / tetrahydrofuran / 0 - 20 °C

1.2: 6 h / Reflux

2.1: N-chloro-succinimide; N,N'-dimethylpiperazine / dichloromethane / 0 °C / Inert atmosphere

2.2: 0 - 20 °C / Inert atmosphere

With N,N'-dimethylpiperazine; pyridine; N-chloro-succinimide; In tetrahydrofuran; dichloromethane;

DOI:10.1016/j.ejmech.2013.03.072

Reference yield:

dimethyl 2-((4-chlorophenyl)(methyl)amino)-1H-indole-3,5-dicarboxylate (1421349-49-6) → methyl 2-chloro-5-methyl-11-(3-(3-phenylureido)propylamino)-5H-indolo[2,3-b]quinoline-9-carboxylate (1445963-13-2)

Guidance literature:

Multi-step reaction with 4 steps

1: diphenylether / 3 h / Reflux

2: trichlorophosphate / 3 h / Reflux

3: tetrahydrofuran / Reflux

4: tetrahydrofuran / 20 °C

With trichlorophosphate; In tetrahydrofuran; diphenylether;

DOI:10.1016/j.ejmech.2013.03.072

upstream raw materials:

dimethyl 1H-indole-3,5-dicarboxylate

N-methyl(p-chloroaniline)

5-methoxycarbonylindole

Downstream raw materials:

methyl 2-chloro-5-methyl-11-(3-(3-phenylureido)propylamino)-5H-indolo[2,3-b]quinoline-9-carboxylate