5-bromo-6-methyl-1-(2-methyl-2H-pyrazol-3-yl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid 4-(N-cyano-S-(methyl)sulfonimidoyl)benzylamide

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Chemical Name:5-bromo-6-methyl-1-(2-methyl-2H-pyrazol-3-yl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid 4-(N-cyano-S-(methyl)sulfonimidoyl)benzylamide
CAS No.:1570078-23-7
Molecular Formula:C₂₀H₁₉BrN₆O₃S
Molecular Weight:503.379
Hs Code.:

Synonyms:5-bromo-6-methyl-1-(2-methyl-2H-pyrazol-3-yl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid 4-(N-cyano-S-(methyl)sulfonimidoyl)benzylamide

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Chemical Property of 5-bromo-6-methyl-1-(2-methyl-2H-pyrazol-3-yl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid 4-(N-cyano-S-(methyl)sulfonimidoyl)benzylamide

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Technology Process of 5-bromo-6-methyl-1-(2-methyl-2H-pyrazol-3-yl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid 4-(N-cyano-S-(methyl)sulfonimidoyl)benzylamide

There total 6 articles about 5-bromo-6-methyl-1-(2-methyl-2H-pyrazol-3-yl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid 4-(N-cyano-S-(methyl)sulfonimidoyl)benzylamide 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: 23.0%

: 1570078-91-9
6-methyl-1-(2-methyl-2H-pyrazol-3-yl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid 4-(N-cyano-S-(methyl)sulfonimidoyl)benzylamide

: 1570078-23-7
5-bromo-6-methyl-1-(2-methyl-2H-pyrazol-3-yl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid 4-(N-cyano-S-(methyl)sulfonimidoyl)benzylamide

Guidance literature:: With N-Bromosuccinimide; acetic acid; In dichloromethane; at 20 ℃; for 18h;

Reference yield:

: 1570082-20-0
[[4-[(1,3-dioxoisoindolin-2-yl)methyl]phenyl]-methyl-λ⁴-sulfanylidene]cyanamide

: 1570078-23-7
5-bromo-6-methyl-1-(2-methyl-2H-pyrazol-3-yl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid 4-(N-cyano-S-(methyl)sulfonimidoyl)benzylamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate; 3-chloro-benzenecarboperoxoic acid / ethanol / 0 - 20 °C

2.1: ethylenediamine / ethanol; acetonitrile; tetrahydrofuran / 5 h / 60 °C

3.1: O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.17 h / 20 °C

3.2: 18 h / 20 °C

4.1: acetic acid; N-Bromosuccinimide / dichloromethane / 18 h / 20 °C

With N-Bromosuccinimide; potassium carbonate; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; acetic acid; ethylenediamine; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 83171-39-5
4-(methylthio)benzylamine

: 1570078-23-7
5-bromo-6-methyl-1-(2-methyl-2H-pyrazol-3-yl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid 4-(N-cyano-S-(methyl)sulfonimidoyl)benzylamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: acetic acid / 3 h / Reflux

2.1: N-Bromosuccinimide; potassium tert-butylate / methanol / 1 h

3.1: potassium carbonate; 3-chloro-benzenecarboperoxoic acid / ethanol / 0 - 20 °C

4.1: ethylenediamine / ethanol; acetonitrile; tetrahydrofuran / 5 h / 60 °C

5.1: O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.17 h / 20 °C

5.2: 18 h / 20 °C

6.1: acetic acid; N-Bromosuccinimide / dichloromethane / 18 h / 20 °C

With N-Bromosuccinimide; potassium tert-butylate; potassium carbonate; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; acetic acid; ethylenediamine; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; methanol; ethanol; dichloromethane; acetic acid; N,N-dimethyl-formamide; acetonitrile;