1-(4-methylbenzamido)-2-[2-(tetrahydro-1H-1-pyrrolyl)acetylamido]anthraquinone

Base Information

Chemical Name:1-(4-methylbenzamido)-2-[2-(tetrahydro-1H-1-pyrrolyl)acetylamido]anthraquinone
CAS No.:1329002-11-0
Molecular Formula:C₂₈H₂₅N₃O₄
Molecular Weight:467.524
Hs Code.:

Synonyms:1-(4-methylbenzamido)-2-[2-(tetrahydro-1H-1-pyrrolyl)acetylamido]anthraquinone

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Chemical Property of 1-(4-methylbenzamido)-2-[2-(tetrahydro-1H-1-pyrrolyl)acetylamido]anthraquinone

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Technology Process of 1-(4-methylbenzamido)-2-[2-(tetrahydro-1H-1-pyrrolyl)acetylamido]anthraquinone

There total 3 articles about 1-(4-methylbenzamido)-2-[2-(tetrahydro-1H-1-pyrrolyl)acetylamido]anthraquinone 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: 39.0%

: 123-75-1
pyrrolidine

: 1329001-66-2
1-(4-methylbenzamido)-2-(chloroacetamido)anthraquinone

: 1329002-11-0
1-(4-methylbenzamido)-2-[2-(tetrahydro-1H-1-pyrrolyl)acetylamido]anthraquinone

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; for 16h; Reflux;

Reference yield:

: 1329001-55-9
1-amino-2-(chloroacetamido)anthraquinone

: 1329002-11-0
1-(4-methylbenzamido)-2-[2-(tetrahydro-1H-1-pyrrolyl)acetylamido]anthraquinone

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / tetrahydrofuran / 3 h / 120 - 130 °C

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 16 h / Reflux

With pyridine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran;

Reference yield:

: 1758-68-5
1,2-diamino-9,10-anthraquinone

: 1329002-11-0
1-(4-methylbenzamido)-2-[2-(tetrahydro-1H-1-pyrrolyl)acetylamido]anthraquinone

Guidance literature:: Multi-step reaction with 3 steps

1: N,N-dimethyl-formamide / 2 h / 20 °C / Inert atmosphere

2: pyridine / tetrahydrofuran / 3 h / 120 - 130 °C

3: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 16 h / Reflux

With pyridine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; N,N-dimethyl-formamide;