N-(3-methyl-2-oxo-1,2,3,4-tetrahydroquinazolin-6-yl)-3-(methylsulfonyl)benzenesulfonamide

Base Information

Chemical Name:N-(3-methyl-2-oxo-1,2,3,4-tetrahydroquinazolin-6-yl)-3-(methylsulfonyl)benzenesulfonamide
CAS No.:1425927-56-5
Molecular Formula:C₁₆H₁₇N₃O₅S₂
Molecular Weight:395.46
Hs Code.:

Synonyms:N-(3-methyl-2-oxo-1,2,3,4-tetrahydroquinazolin-6-yl)-3-(methylsulfonyl)benzenesulfonamide

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Chemical Property of N-(3-methyl-2-oxo-1,2,3,4-tetrahydroquinazolin-6-yl)-3-(methylsulfonyl)benzenesulfonamide

Chemical Property:

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Technology Process of N-(3-methyl-2-oxo-1,2,3,4-tetrahydroquinazolin-6-yl)-3-(methylsulfonyl)benzenesulfonamide

There total 3 articles about N-(3-methyl-2-oxo-1,2,3,4-tetrahydroquinazolin-6-yl)-3-(methylsulfonyl)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:

: 5335-40-0
3-(methylsulfonyl)benzenesulfonyl chloride

: 1410782-55-6
6-amino-3-methyl-3,4-dihydroquinazolin-2(1H)-one

: 1425927-56-5
N-(3-methyl-2-oxo-1,2,3,4-tetrahydroquinazolin-6-yl)-3-(methylsulfonyl)benzenesulfonamide

Guidance literature:: With pyridine; dmap; at 60 ℃; for 16h;

Reference yield:

: 1253226-04-8
3-methyl-6-nitro-3,4-dihydroquinazolin-2(1H)-one

: 1425927-56-5
N-(3-methyl-2-oxo-1,2,3,4-tetrahydroquinazolin-6-yl)-3-(methylsulfonyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen; acetic acid / 16 h / 1551.49 Torr

2: dmap; pyridine / 16 h / 60 °C

With pyridine; dmap; hydrogen; acetic acid;

Reference yield:

: 24365-65-9
3-methyl-3,4-dihydro-2(1H)-quinazolinone

: 1425927-56-5
N-(3-methyl-2-oxo-1,2,3,4-tetrahydroquinazolin-6-yl)-3-(methylsulfonyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: sulfuric acid; potassium nitrate / 3 h / 20 °C / Cooling with ice

2: hydrogen; acetic acid / 16 h / 1551.49 Torr

3: dmap; pyridine / 16 h / 60 °C

With pyridine; dmap; sulfuric acid; hydrogen; acetic acid; potassium nitrate;