N-(4-((4-(N-carbamimidoylsulfamoyl)phenyl)amino)quinazolin-6-yl)acrylamide

Base Information

Chemical Name:N-(4-((4-(N-carbamimidoylsulfamoyl)phenyl)amino)quinazolin-6-yl)acrylamide
CAS No.:1474030-85-7
Molecular Formula:C₁₈H₁₇N₇O₃S
Molecular Weight:411.444
Hs Code.:

Synonyms:N-(4-((4-(N-carbamimidoylsulfamoyl)phenyl)amino)quinazolin-6-yl)acrylamide

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Chemical Property of N-(4-((4-(N-carbamimidoylsulfamoyl)phenyl)amino)quinazolin-6-yl)acrylamide

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Technology Process of N-(4-((4-(N-carbamimidoylsulfamoyl)phenyl)amino)quinazolin-6-yl)acrylamide

There total 4 articles about N-(4-((4-(N-carbamimidoylsulfamoyl)phenyl)amino)quinazolin-6-yl)acrylamide 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: 55.0%

: 1474030-70-0
4-((6-aminoquinazolin-4-yl)amino)-N-carbamimidoylbenzenesulfonamide

: 814-68-6,25189-84-8
acryloyl chloride

: 1474030-85-7
N-(4-((4-(N-carbamimidoylsulfamoyl)phenyl)amino)quinazolin-6-yl)acrylamide

Guidance literature:: With sodium hydrogencarbonate; In N,N-dimethyl-formamide; at 0 ℃; for 0.5h; Inert atmosphere;
DOI:10.1039/c3md00118k

Reference yield:

: 17420-30-3
5-nitroanthranilonitrile

: 1474030-85-7
N-(4-((4-(N-carbamimidoylsulfamoyl)phenyl)amino)quinazolin-6-yl)acrylamide

Guidance literature:: Multi-step reaction with 4 steps

1: acetic anhydride / 24 h / Reflux

2: acetic acid / 1 h / Reflux

3: methanol; tin(ll) chloride / 1 h / Inert atmosphere; Reflux

4: sodium hydrogencarbonate / N,N-dimethyl-formamide / 0.5 h / 0 °C / Inert atmosphere

With methanol; acetic anhydride; sodium hydrogencarbonate; acetic acid; tin(ll) chloride; In N,N-dimethyl-formamide; 2: |Dimroth Rearrangement;
DOI:10.1039/c3md00118k

Reference yield:

: 1474030-59-5
N-carbamimidoyl-4-[(6-nitroquinazolin-4-yl)amino]benzene-1-sulfonamide

: 1474030-85-7
N-(4-((4-(N-carbamimidoylsulfamoyl)phenyl)amino)quinazolin-6-yl)acrylamide

Guidance literature:: Multi-step reaction with 2 steps

1: methanol; tin(ll) chloride / 1 h / Inert atmosphere; Reflux

2: sodium hydrogencarbonate / N,N-dimethyl-formamide / 0.5 h / 0 °C / Inert atmosphere

With methanol; sodium hydrogencarbonate; tin(ll) chloride; In N,N-dimethyl-formamide;
DOI:10.1039/c3md00118k