N-[2-chloro-4-fluoro-5-(3-methyl-5-oxo-4-vinyl-4,5-dihydro-[1,2,4]triazol-1-yl)-phenyl]-N-methyl-methanesulfonamide

Base Information

Chemical Name:N-[2-chloro-4-fluoro-5-(3-methyl-5-oxo-4-vinyl-4,5-dihydro-[1,2,4]triazol-1-yl)-phenyl]-N-methyl-methanesulfonamide
CAS No.:220063-01-4
Molecular Formula:C₁₃H₁₄ClFN₄O₃S
Molecular Weight:360.797
Hs Code.:

<i>N</i>-[2-chloro-4-fluoro-5-(3-methyl-5-oxo-4-vinyl-4,5-dihydro-[1,2,4]triazol-1-yl)-phenyl]-<i>N</i>-methyl-methanesulfonamide

Synonyms:N-[2-chloro-4-fluoro-5-(3-methyl-5-oxo-4-vinyl-4,5-dihydro-[1,2,4]triazol-1-yl)-phenyl]-N-methyl-methanesulfonamide

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Chemical Property of N-[2-chloro-4-fluoro-5-(3-methyl-5-oxo-4-vinyl-4,5-dihydro-[1,2,4]triazol-1-yl)-phenyl]-N-methyl-methanesulfonamide

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Technology Process of N-[2-chloro-4-fluoro-5-(3-methyl-5-oxo-4-vinyl-4,5-dihydro-[1,2,4]triazol-1-yl)-phenyl]-N-methyl-methanesulfonamide

There total 7 articles about N-[2-chloro-4-fluoro-5-(3-methyl-5-oxo-4-vinyl-4,5-dihydro-[1,2,4]triazol-1-yl)-phenyl]-N-methyl-methanesulfonamide 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: 81.0%

: 220063-00-3
N-{5-[4-(2-bromo-ethyl)-3-methyl-5-oxo-4,5-dihydro-[1,2,4]triazol-1-yl]-2-chloro-4-fluoro-phenyl}-N-methyl-methanesulfonamide

: 220063-01-4
N-[2-chloro-4-fluoro-5-(3-methyl-5-oxo-4-vinyl-4,5-dihydro-[1,2,4]triazol-1-yl)-phenyl]-N-methyl-methanesulfonamide

Guidance literature:: With potassium carbonate; sodium iodide; In N,N-dimethyl-formamide; at 80 ℃; for 18h;
DOI:10.1016/S0040-4039(98)02111-X

Reference yield:

: 111992-04-2
4,5-dihydro-1-(4-chloro-2-fluorophenyl)-3-methyl-5-oxo-1H-1,2,4-triazole

: 220063-01-4
N-[2-chloro-4-fluoro-5-(3-methyl-5-oxo-4-vinyl-4,5-dihydro-[1,2,4]triazol-1-yl)-phenyl]-N-methyl-methanesulfonamide

Guidance literature:: Multi-step reaction with 7 steps

1: 82 percent / K₂CO₃, NaI / dimethylformamide / 4 h / 80 °C

2: HNO₃, H₂SO₄ / 82 h / 10 °C

3: 85 percent / H₂ / PtO₂

4: 85 percent / pyridine

5: 90 percent / NaH

6: 97 percent / boron tribromide / CH₂Cl₂ / 0.5 h / 10 °C

7: 81 percent / potasium carbonate, sodium iodide / dimethylformamide / 18 h / 80 °C

With pyridine; sulfuric acid; hydrogen; nitric acid; boron tribromide; sodium hydride; potassium carbonate; sodium iodide; platinum(IV) oxide; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(98)02111-X

Reference yield:

: 220062-95-3
2-(4-chloro-2-fluoro-phenyl)-4-(2-fluoro-ethyl)-5-methyl-2,4-dihydro-[1,2,4]triazol-3-one

: 220063-01-4
N-[2-chloro-4-fluoro-5-(3-methyl-5-oxo-4-vinyl-4,5-dihydro-[1,2,4]triazol-1-yl)-phenyl]-N-methyl-methanesulfonamide

Guidance literature:: Multi-step reaction with 6 steps

1: HNO₃, H₂SO₄ / 82 h / 10 °C

2: 85 percent / H₂ / PtO₂

3: 85 percent / pyridine

4: 90 percent / NaH

5: 97 percent / boron tribromide / CH₂Cl₂ / 0.5 h / 10 °C

6: 81 percent / potasium carbonate, sodium iodide / dimethylformamide / 18 h / 80 °C

With pyridine; sulfuric acid; hydrogen; nitric acid; boron tribromide; sodium hydride; potassium carbonate; sodium iodide; platinum(IV) oxide; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(98)02111-X