ethyl 1-(4-bromophenyl)-3-{[(4-cyanophenyl)acetyl]amino}-1H-pyrrole-2-carboxylate

Base Information

Chemical Name:ethyl 1-(4-bromophenyl)-3-{[(4-cyanophenyl)acetyl]amino}-1H-pyrrole-2-carboxylate
CAS No.:1272674-07-3
Molecular Formula:C₂₂H₁₈BrN₃O₃
Molecular Weight:452.307
Hs Code.:

Synonyms:ethyl 1-(4-bromophenyl)-3-{[(4-cyanophenyl)acetyl]amino}-1H-pyrrole-2-carboxylate

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Chemical Property of ethyl 1-(4-bromophenyl)-3-{[(4-cyanophenyl)acetyl]amino}-1H-pyrrole-2-carboxylate

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Technology Process of ethyl 1-(4-bromophenyl)-3-{[(4-cyanophenyl)acetyl]amino}-1H-pyrrole-2-carboxylate

There total 1 articles about ethyl 1-(4-bromophenyl)-3-{[(4-cyanophenyl)acetyl]amino}-1H-pyrrole-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: 49.9%

: 5462-71-5
4-cyanophenylacetic acid

: 1272673-95-6
ethyl 3-amino-1-(4-bromophenyl)-1H-pyrrole-2-carboxylate hydrochloride

: 1272674-07-3
ethyl 1-(4-bromophenyl)-3-{[(4-cyanophenyl)acetyl]amino}-1H-pyrrole-2-carboxylate

Guidance literature:: With triethylamine; dicyclohexyl-carbodiimide; In acetonitrile; at 20 ℃;

Reference yield: 64.2%

: 1272674-07-3
ethyl 1-(4-bromophenyl)-3-{[(4-cyanophenyl)acetyl]amino}-1H-pyrrole-2-carboxylate

: 1272674-08-4
4-[1-(4-bromophenyl)-7-hydroxy-5-oxo-4,5-dihydro-1H-pyrrolo[3,2-b]pyridin-6-yl]benzonitrile

Guidance literature:: With potassium tert-butylate; In dimethyl sulfoxide; at 100 ℃;

Reference yield:

: 1272674-07-3
ethyl 1-(4-bromophenyl)-3-{[(4-cyanophenyl)acetyl]amino}-1H-pyrrole-2-carboxylate

: 1272672-40-8
4-[7-hydroxy-1-(2'-hydroxy-4-biphenylyl)-5-oxo-4,5-dihydro-1H-pyrrolo[3,2-b]pyridin-6-yl]benzonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: potassium tert-butylate / dimethyl sulfoxide / 100 °C

2: caesium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 0.33 h / 130 °C / Inert atmosphere; Biotage Initiator

With potassium tert-butylate; caesium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; water; dimethyl sulfoxide;