N-carbamimidoyl-4-[(6-nitroquinazolin-4-yl)amino]benzene-1-sulfonamide

Base Information

Chemical Name:N-carbamimidoyl-4-[(6-nitroquinazolin-4-yl)amino]benzene-1-sulfonamide
CAS No.:1474030-59-5
Molecular Formula:C₁₅H₁₃N₇O₄S
Molecular Weight:387.379
Hs Code.:

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

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Chemical Property of N-carbamimidoyl-4-[(6-nitroquinazolin-4-yl)amino]benzene-1-sulfonamide

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Technology Process of N-carbamimidoyl-4-[(6-nitroquinazolin-4-yl)amino]benzene-1-sulfonamide

There total 3 articles about N-carbamimidoyl-4-[(6-nitroquinazolin-4-yl)amino]benzene-1-sulfonamide 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: 75.0%

: 22363-16-2
ethyl N-(2-cyano-4-nitrophenyl)formimidate

: 57-67-0,61116-95-8
1-amino-4-({[amino(imino)methyl]amino}sulfonyl)benzene

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

Guidance literature:: With acetic acid; for 1h; Reflux;
DOI:10.1039/c3md00118k

Reference yield: 58.0%

: 39263-34-8
N′-(2-cyano-4-nitrophenyl)-N,N-dimethylformimidamide

: 57-67-0,61116-95-8
1-amino-4-({[amino(imino)methyl]amino}sulfonyl)benzene

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

Guidance literature:: In acetic acid; for 3h; Reflux;
DOI:10.1002/cbdv.202000237

Reference yield:

: 17420-30-3
5-nitroanthranilonitrile

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

Guidance literature:: Multi-step reaction with 2 steps

1: acetic anhydride / 24 h / Reflux

2: acetic acid / 1 h / Reflux

With acetic anhydride; acetic acid; 2: |Dimroth Rearrangement;
DOI:10.1039/c3md00118k