ethyl 5-(2-(tert-butylamino)-2-oxo-1-p-tolylethyl)-4-oxo-3-propyl-4,5-dihydro-1H-pyrrolo[3,2-c]quinoline-2-carboxylate

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Chemical Name:ethyl 5-(2-(tert-butylamino)-2-oxo-1-p-tolylethyl)-4-oxo-3-propyl-4,5-dihydro-1H-pyrrolo[3,2-c]quinoline-2-carboxylate
CAS No.:1310373-01-3
Molecular Formula:C₃₀H₃₅N₃O₄
Molecular Weight:501.626
Hs Code.:

Synonyms:ethyl 5-(2-(tert-butylamino)-2-oxo-1-p-tolylethyl)-4-oxo-3-propyl-4,5-dihydro-1H-pyrrolo[3,2-c]quinoline-2-carboxylate

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Chemical Property of ethyl 5-(2-(tert-butylamino)-2-oxo-1-p-tolylethyl)-4-oxo-3-propyl-4,5-dihydro-1H-pyrrolo[3,2-c]quinoline-2-carboxylate

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Technology Process of ethyl 5-(2-(tert-butylamino)-2-oxo-1-p-tolylethyl)-4-oxo-3-propyl-4,5-dihydro-1H-pyrrolo[3,2-c]quinoline-2-carboxylate

There total 2 articles about ethyl 5-(2-(tert-butylamino)-2-oxo-1-p-tolylethyl)-4-oxo-3-propyl-4,5-dihydro-1H-pyrrolo[3,2-c]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: 65.0%

: 2999-46-4
Ethyl isocyanoacetate

: 1322565-41-2
C₂₅H₂₉IN₂O₂

: 1310373-01-3
ethyl 5-(2-(tert-butylamino)-2-oxo-1-p-tolylethyl)-4-oxo-3-propyl-4,5-dihydro-1H-pyrrolo[3,2-c]quinoline-2-carboxylate

Guidance literature:: With copper(l) iodide; caesium carbonate; In N,N-dimethyl-formamide; at 130 ℃; for 0.166667h;
DOI:10.1021/jo2006939

Reference yield:

: 764-33-0
hex-2-ynoic acid

: 119072-55-8,7188-38-7
tert-butylisonitrile

: 615-43-0
2-iodophenylamine

: 104-87-0
4-methyl-benzaldehyde

: 1310373-01-3
ethyl 5-(2-(tert-butylamino)-2-oxo-1-p-tolylethyl)-4-oxo-3-propyl-4,5-dihydro-1H-pyrrolo[3,2-c]quinoline-2-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: methanol / 0.5 h / 20 °C

1.2: 0.25 h / 20 °C

1.3: 24 h / 20 °C

2.1: copper(l) iodide; caesium carbonate / N,N-dimethyl-formamide / 0.17 h / 130 °C

With copper(l) iodide; caesium carbonate; In methanol; N,N-dimethyl-formamide; 1.1: Ugi condensation / 1.2: Ugi condensation / 1.3: Ugi condensation;
DOI:10.1021/jo2006939