p-{13-amino-3-(p-bromophenyl)-12-ethoxycarbonyl-5,7,9,10,14-pentazatricyclo [7.5.0.0^2,6]tetradeca-1⁽¹⁴⁾,2⁽⁶⁾,3,7,10,12-hexaen-5-yl}benzenesulfonamide

Base Information

• Chemical Name: p-{13-amino-3-(p-bromophenyl)-12-ethoxycarbonyl-5,7,9,10,14-pentazatricyclo [7.5.0.0^2,6]tetradeca-1⁽¹⁴⁾,2⁽⁶⁾,3,7,10,12-hexaen-5-yl}benzenesulfonamide
• CAS No.: 1616063-75-2
• Molecular Formula: C₂₄H₂₀BrN₇O₄S
• Molecular Weight: 582.437

Synonyms:p-{13-amino-3-(p-bromophenyl)-12-ethoxycarbonyl-5,7,9,10,14-pentazatricyclo [7.5.0.0^2,6]tetradeca-1⁽¹⁴⁾,2⁽⁶⁾,3,7,10,12-hexaen-5-yl}benzenesulfonamide

Chemical Property of p-{13-amino-3-(p-bromophenyl)-12-ethoxycarbonyl-5,7,9,10,14-pentazatricyclo [7.5.0.0^2,6]tetradeca-1⁽¹⁴⁾,2⁽⁶⁾,3,7,10,12-hexaen-5-yl}benzenesulfonamide

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Technology Process of p-{13-amino-3-(p-bromophenyl)-12-ethoxycarbonyl-5,7,9,10,14-pentazatricyclo [7.5.0.0^2,6]tetradeca-1⁽¹⁴⁾,2⁽⁶⁾,3,7,10,12-hexaen-5-yl}benzenesulfonamide

There total 6 articles about p-{13-amino-3-(p-bromophenyl)-12-ethoxycarbonyl-5,7,9,10,14-pentazatricyclo [7.5.0.0^2,6]tetradeca-1⁽¹⁴⁾,2⁽⁶⁾,3,7,10,12-hexaen-5-yl}benzenesulfonamide 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: 90.0%

4-(3-amino-5-(4-bromophenyl)-4-imino-3,4-dihydropyrrolo[2,3-d]pyrimidin-7-yl)benzenesulfonamide (1616063-62-7) + ethyl (ethoxymethylene)cyanoacetate (94-05-3,42466-69-3) → p-{13-amino-3-(p-bromophenyl)-12-ethoxycarbonyl-5,7,9,10,14-pentazatricyclo [7.5.0.02,6]tetradeca-1(14),2(6),3,7,10,12-hexaen-5-yl}benzenesulfonamide (1616063-75-2)

Guidance literature:

In ethanol; for 8h; Reflux;

DOI:10.1016/j.bmc.2014.05.009

Reference yield:

4-(2-(4-bromophenyl)-2-oxoethylamino)benzenesulfonamide (1616063-57-0) → p-{13-amino-3-(p-bromophenyl)-12-ethoxycarbonyl-5,7,9,10,14-pentazatricyclo [7.5.0.02,6]tetradeca-1(14),2(6),3,7,10,12-hexaen-5-yl}benzenesulfonamide (1616063-75-2)

Guidance literature:

Multi-step reaction with 4 steps

1: sodium ethanolate / ethanol / 8 h / Reflux

2: 6 h / Reflux

3: hydrazine hydrate / ethanol / 1 h / 20 °C

4: ethanol / 8 h / Reflux

With sodium ethanolate; hydrazine hydrate; In ethanol;

DOI:10.1016/j.bmc.2014.05.009

Reference yield:

4-(2-amino-4-(4-bromophenyl)-3-cyano-1H-pyrrol-1-yl)benzenesulfonamide (1616063-59-2) → p-{13-amino-3-(p-bromophenyl)-12-ethoxycarbonyl-5,7,9,10,14-pentazatricyclo [7.5.0.02,6]tetradeca-1(14),2(6),3,7,10,12-hexaen-5-yl}benzenesulfonamide (1616063-75-2)

Guidance literature:

Multi-step reaction with 3 steps

1: 6 h / Reflux

2: hydrazine hydrate / ethanol / 1 h / 20 °C

3: ethanol / 8 h / Reflux

With hydrazine hydrate; In ethanol;

DOI:10.1016/j.bmc.2014.05.009

upstream raw materials:

4-(2-(4-bromophenyl)-2-oxoethylamino)benzenesulfonamide

4-(2-amino-4-(4-bromophenyl)-3-cyano-1H-pyrrol-1-yl)benzenesulfonamide

ethyl N-(4-(4-bromophenyl)-3-cyano-1-(4-sulfamoylphenyl)-1H-pyrrol-2-yl)formimidate

4-(3-amino-5-(4-bromophenyl)-4-imino-3,4-dihydropyrrolo[2,3-d]pyrimidin-7-yl)benzenesulfonamide

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