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

Base Information

Chemical Name:methyl 9-bromo-5-methyl-11-(3-(3-phenylureido)propylamino)-5H-indolo[2,3-b]quinoline-2-carboxylate
CAS No.:1445963-15-4
Molecular Formula:C₂₈H₂₆BrN₅O₃
Molecular Weight:560.45
Hs Code.:

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

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Chemical Property of methyl 9-bromo-5-methyl-11-(3-(3-phenylureido)propylamino)-5H-indolo[2,3-b]quinoline-2-carboxylate

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Technology Process of methyl 9-bromo-5-methyl-11-(3-(3-phenylureido)propylamino)-5H-indolo[2,3-b]quinoline-2-carboxylate

There total 7 articles about methyl 9-bromo-5-methyl-11-(3-(3-phenylureido)propylamino)-5H-indolo[2,3-b]quinoline-2-carboxylate 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: 83.0%

: 1421349-41-8
methyl 11-(3-aminopropylamino)-9-bromo-5-methyl-5H-indolo[2,3-b]quinoline-2-carboxylate

: 103-71-9
phenyl isocyanate

: 1445963-15-4
methyl 9-bromo-5-methyl-11-(3-(3-phenylureido)propylamino)-5H-indolo[2,3-b]quinoline-2-carboxylate

Guidance literature:: In tetrahydrofuran; at 20 ℃;
DOI:10.1016/j.ejmech.2013.03.072

Reference yield:

: 10075-50-0
5-bromo-1H-indole

: 1445963-15-4
methyl 9-bromo-5-methyl-11-(3-(3-phenylureido)propylamino)-5H-indolo[2,3-b]quinoline-2-carboxylate

Guidance literature:: Multi-step reaction with 6 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

3.1: diphenylether / 3 h / Reflux

4.1: trichlorophosphate / 3 h / Reflux

5.1: tetrahydrofuran / Reflux

6.1: tetrahydrofuran / 20 °C

With N,N'-dimethylpiperazine; pyridine; N-chloro-succinimide; trichlorophosphate; In tetrahydrofuran; diphenylether; dichloromethane;
DOI:10.1016/j.ejmech.2013.03.072

Reference yield:

: 1421349-57-6
methyl 9-bromo-5-methyl-11-oxo-6,11-dihydro-5H-indolo[2,3-b]quinoline-2-carboxylate

: 1445963-15-4
methyl 9-bromo-5-methyl-11-(3-(3-phenylureido)propylamino)-5H-indolo[2,3-b]quinoline-2-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: trichlorophosphate / 3 h / Reflux

2: tetrahydrofuran / Reflux

3: tetrahydrofuran / 20 °C

With trichlorophosphate; In tetrahydrofuran;
DOI:10.1016/j.ejmech.2013.03.072