4-amino-N-[2-(4-chlorophenyl)-4-oxoquinazolin-3(4H)-yl]benzenesulfonamide

Base Information

Chemical Name:4-amino-N-[2-(4-chlorophenyl)-4-oxoquinazolin-3(4H)-yl]benzenesulfonamide
CAS No.:1314603-07-0
Molecular Formula:C₂₀H₁₅ClN₄O₃S
Molecular Weight:426.883
Hs Code.:

Synonyms:4-amino-N-[2-(4-chlorophenyl)-4-oxoquinazolin-3(4H)-yl]benzenesulfonamide

Suppliers and Price of 4-amino-N-[2-(4-chlorophenyl)-4-oxoquinazolin-3(4H)-yl]benzenesulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-amino-N-[2-(4-chlorophenyl)-4-oxoquinazolin-3(4H)-yl]benzenesulfonamide

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Technology Process of 4-amino-N-[2-(4-chlorophenyl)-4-oxoquinazolin-3(4H)-yl]benzenesulfonamide

There total 2 articles about 4-amino-N-[2-(4-chlorophenyl)-4-oxoquinazolin-3(4H)-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: 75.0%

: 1314602-98-6
C₂₂H₁₇ClN₄O₄S

: 1314603-07-0
4-amino-N-[2-(4-chlorophenyl)-4-oxoquinazolin-3(4H)-yl]benzenesulfonamide

Guidance literature:: With hydrogenchloride; water; In ethanol; for 0.0333333h; Microwave irradiation;
DOI:10.3998/ark.5550190.0012.916

Reference yield:

: 34425-87-1
N-(4-chlorobenzoyl)anthranilic acid

: 3989-50-2
4-acetamidobenzenesulfonylhydrazine

: 1314603-07-0
4-amino-N-[2-(4-chlorophenyl)-4-oxoquinazolin-3(4H)-yl]benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: phosphorus trichloride / tetrahydrofuran / 0.4 h / Microwave irradiation

2: hydrogenchloride; water / ethanol / 0.03 h / Microwave irradiation

With hydrogenchloride; water; phosphorus trichloride; In tetrahydrofuran; ethanol;
DOI:10.3998/ark.5550190.0012.916