3-[3-(5-{[(5-fluoropyridin-2-yl)oxy]methyl}-1-methyl-1H-pyrazol-4-yl)-1,2-oxazol-5-yl]benzenesulfonamide

Base Information

Chemical Name:3-[3-(5-{[(5-fluoropyridin-2-yl)oxy]methyl}-1-methyl-1H-pyrazol-4-yl)-1,2-oxazol-5-yl]benzenesulfonamide
CAS No.:1359028-76-4
Molecular Formula:C₁₉H₁₆FN₅O₄S
Molecular Weight:429.432
Hs Code.:

Synonyms:3-[3-(5-{[(5-fluoropyridin-2-yl)oxy]methyl}-1-methyl-1H-pyrazol-4-yl)-1,2-oxazol-5-yl]benzenesulfonamide

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Chemical Property of 3-[3-(5-{[(5-fluoropyridin-2-yl)oxy]methyl}-1-methyl-1H-pyrazol-4-yl)-1,2-oxazol-5-yl]benzenesulfonamide

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Technology Process of 3-[3-(5-{[(5-fluoropyridin-2-yl)oxy]methyl}-1-methyl-1H-pyrazol-4-yl)-1,2-oxazol-5-yl]benzenesulfonamide

There total 7 articles about 3-[3-(5-{[(5-fluoropyridin-2-yl)oxy]methyl}-1-methyl-1H-pyrazol-4-yl)-1,2-oxazol-5-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:

: 1310456-99-5
3-ethynylbenzenesulfonamide

: 1359030-09-3
5-{[(5-fluoropyridin-2-yl)oxy]methyl}-N-hydroxy-1-methyl-1H-pyrazole-4-carboximidoyl chloride

: 1359028-76-4
3-[3-(5-{[(5-fluoropyridin-2-yl)oxy]methyl}-1-methyl-1H-pyrazol-4-yl)-1,2-oxazol-5-yl]benzenesulfonamide

Guidance literature:: With triethylamine; In tetrahydrofuran; toluene; at 60 ℃; for 2h;

Reference yield:

: 81303-64-2
ethyl 5-(hydroxymethyl)-1-methyl-1H-pyrazole-4-carboxylate

: 1359028-76-4
3-[3-(5-{[(5-fluoropyridin-2-yl)oxy]methyl}-1-methyl-1H-pyrazol-4-yl)-1,2-oxazol-5-yl]benzenesulfonamide

Guidance literature:: Multi-step reaction with 6 steps

1: caesium carbonate; palladium diacetate; racemic-2-(di-tert-butylphosphino)-1,1′-binaphthyl / 1,4-dioxane / 1 h / 100 °C / Inert atmosphere

2: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 20 °C / Inert atmosphere; Cooling with ice

3: manganese(IV) oxide / chloroform / 64 h / 20 °C

4: hydroxylamine / methanol; water / 16 h / 20 °C

5: tert-butylhypochlorite / chloroform; tetrachloromethane / 2 h / 20 °C

6: triethylamine / tetrahydrofuran; toluene / 2 h / 60 °C

With racemic-2-(di-tert-butylphosphino)-1,1′-binaphthyl; manganese(IV) oxide; lithium aluminium tetrahydride; tert-butylhypochlorite; hydroxylamine; palladium diacetate; caesium carbonate; triethylamine; In tetrahydrofuran; 1,4-dioxane; methanol; tetrachloromethane; chloroform; water; toluene;

Reference yield:

: 1359030-10-6
(5-{[(5-fluoropyridin-2-yl)oxy]methyl}-1-methyl-1H-pyrazole-4-yl)methanol

: 1359028-76-4
3-[3-(5-{[(5-fluoropyridin-2-yl)oxy]methyl}-1-methyl-1H-pyrazol-4-yl)-1,2-oxazol-5-yl]benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: manganese(IV) oxide / chloroform / 64 h / 20 °C

2: hydroxylamine / methanol; water / 16 h / 20 °C

3: tert-butylhypochlorite / chloroform; tetrachloromethane / 2 h / 20 °C

4: triethylamine / tetrahydrofuran; toluene / 2 h / 60 °C

With manganese(IV) oxide; tert-butylhypochlorite; hydroxylamine; triethylamine; In tetrahydrofuran; methanol; tetrachloromethane; chloroform; water; toluene;