3-bromo-N-(3,4-dichlorobenzyl)-N-(2-(dimethylamino)ethyl)-4-(4-fluorophenyl)-4H-thieno[3,2-b]pyrrole-5-carboxamide

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Chemical Name:3-bromo-N-(3,4-dichlorobenzyl)-N-(2-(dimethylamino)ethyl)-4-(4-fluorophenyl)-4H-thieno[3,2-b]pyrrole-5-carboxamide
CAS No.:1450743-08-4
Molecular Formula:C₂₄H₂₁BrCl₂FN₃OS
Molecular Weight:569.325
Hs Code.:

Synonyms:3-bromo-N-(3,4-dichlorobenzyl)-N-(2-(dimethylamino)ethyl)-4-(4-fluorophenyl)-4H-thieno[3,2-b]pyrrole-5-carboxamide

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Chemical Property of 3-bromo-N-(3,4-dichlorobenzyl)-N-(2-(dimethylamino)ethyl)-4-(4-fluorophenyl)-4H-thieno[3,2-b]pyrrole-5-carboxamide

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Technology Process of 3-bromo-N-(3,4-dichlorobenzyl)-N-(2-(dimethylamino)ethyl)-4-(4-fluorophenyl)-4H-thieno[3,2-b]pyrrole-5-carboxamide

There total 5 articles about 3-bromo-N-(3,4-dichlorobenzyl)-N-(2-(dimethylamino)ethyl)-4-(4-fluorophenyl)-4H-thieno[3,2-b]pyrrole-5-carboxamide 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: 95.0%

: 1450743-07-3
ethyl 3-bromo-4-(4-fluorophenyl)-4H-thieno[3,2-b]pyrrole-5-carboxylic acid

: 91429-04-8
N'-(3,4-dichlorobenzyl)-N,N-dimethylethane-1,2-diamine

: 1450743-08-4
3-bromo-N-(3,4-dichlorobenzyl)-N-(2-(dimethylamino)ethyl)-4-(4-fluorophenyl)-4H-thieno[3,2-b]pyrrole-5-carboxamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 20 ℃; for 30h;
DOI:10.1016/j.bmc.2013.05.067

Reference yield:

: 18791-75-8
4-Bromothiophen-2-aldehyde

: 1450743-08-4
3-bromo-N-(3,4-dichlorobenzyl)-N-(2-(dimethylamino)ethyl)-4-(4-fluorophenyl)-4H-thieno[3,2-b]pyrrole-5-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: sodium ethanolate / ethanol / 2.5 h / -10 - 20 °C

2: 5,5-dimethyl-1,3-cyclohexadiene / 2 h / 120 °C

3: copper diacetate; triethylamine; pyridine / 21 h / 20 °C / Molecular sieve

4: sodium hydroxide / tetrahydrofuran; ethanol / 2.5 h / 65 - 75 °C

5: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 30 h / 20 °C

With pyridine; sodium ethanolate; copper diacetate; triethylamine; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; sodium hydroxide; In tetrahydrofuran; 5,5-dimethyl-1,3-cyclohexadiene; ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2013.05.067

Reference yield:

: 934246-45-4
ethyl 2-azido-3-(4-bromo-2-thienyl)acrylate

: 1450743-08-4
3-bromo-N-(3,4-dichlorobenzyl)-N-(2-(dimethylamino)ethyl)-4-(4-fluorophenyl)-4H-thieno[3,2-b]pyrrole-5-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: 5,5-dimethyl-1,3-cyclohexadiene / 2 h / 120 °C

2: copper diacetate; triethylamine; pyridine / 21 h / 20 °C / Molecular sieve

3: sodium hydroxide / tetrahydrofuran; ethanol / 2.5 h / 65 - 75 °C

4: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 30 h / 20 °C

With pyridine; copper diacetate; triethylamine; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; sodium hydroxide; In tetrahydrofuran; 5,5-dimethyl-1,3-cyclohexadiene; ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2013.05.067