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(S)-N-(4-(3-fluoro-4-(trifluoromethoxy)phenyl)-3,4-dihydro-2H-pyrano[3,2-b]pyridin-4-yl)benzenesulfonamide 2,2,2-trifluoroacetate

Base Information Edit
  • Chemical Name:(S)-N-(4-(3-fluoro-4-(trifluoromethoxy)phenyl)-3,4-dihydro-2H-pyrano[3,2-b]pyridin-4-yl)benzenesulfonamide 2,2,2-trifluoroacetate
  • CAS No.:1561765-64-7
  • Molecular Formula:C2HF3O2*C21H16F4N2O4S
  • Molecular Weight:582.453
  • Hs Code.:
  • Mol file:1561765-64-7.mol
(S)-N-(4-(3-fluoro-4-(trifluoromethoxy)phenyl)-3,4-dihydro-2H-pyrano[3,2-b]pyridin-4-yl)benzenesulfonamide 2,2,2-trifluoroacetate

Synonyms:(S)-N-(4-(3-fluoro-4-(trifluoromethoxy)phenyl)-3,4-dihydro-2H-pyrano[3,2-b]pyridin-4-yl)benzenesulfonamide 2,2,2-trifluoroacetate

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Chemical Property of (S)-N-(4-(3-fluoro-4-(trifluoromethoxy)phenyl)-3,4-dihydro-2H-pyrano[3,2-b]pyridin-4-yl)benzenesulfonamide 2,2,2-trifluoroacetate Edit
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Technology Process of (S)-N-(4-(3-fluoro-4-(trifluoromethoxy)phenyl)-3,4-dihydro-2H-pyrano[3,2-b]pyridin-4-yl)benzenesulfonamide 2,2,2-trifluoroacetate

There total 7 articles about (S)-N-(4-(3-fluoro-4-(trifluoromethoxy)phenyl)-3,4-dihydro-2H-pyrano[3,2-b]pyridin-4-yl)benzenesulfonamide 2,2,2-trifluoroacetate 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:
Guidance literature:
(S)-4-(3-fluoro-4-(trifluoromethoxy)phenyl)-3,4-dihydro-2H-pyrano[3,2-b]pyridin-4-amine hydrochloride; benzenesulfonyl chloride; With triethylamine; In dichloromethane; at 20 ℃; for 18h;
trifluoroacetic acid; In dichloromethane; water; acetonitrile;
Guidance literature:
Multi-step reaction with 6 steps
1.1: triphenylphosphine; palladium diacetate; potassium acetate; tetraethylammonium chloride / N,N-dimethyl-formamide / 16 h / 110 °C / Inert atmosphere
2.1: sodium hydrogencarbonate; ozone / methanol; chloroform / 16 h / -78 °C
2.2: 12 h / -78 - 20 °C
3.1: titanium(IV) tetraethanolate / 2-methyltetrahydrofuran / 4 h / 20 °C
4.1: magnesium; iodine / 2-methyltetrahydrofuran / 0.5 h / 35 °C
4.2: Cooling with acetone-dry ice
5.1: hydrogenchloride / ethanol; 1,4-dioxane / 2 h / 20 °C
6.1: triethylamine / dichloromethane / 18 h / 20 °C
With hydrogenchloride; titanium(IV) tetraethanolate; tetraethylammonium chloride; iodine; potassium acetate; palladium diacetate; sodium hydrogencarbonate; ozone; magnesium; triethylamine; triphenylphosphine; In 2-methyltetrahydrofuran; 1,4-dioxane; methanol; ethanol; dichloromethane; chloroform; N,N-dimethyl-formamide; 4.1: |Grignard Reaction / 4.2: |Grignard Reaction;
Guidance literature:
Multi-step reaction with 4 steps
1.1: titanium(IV) tetraethanolate / 2-methyltetrahydrofuran / 4 h / 20 °C
2.1: magnesium; iodine / 2-methyltetrahydrofuran / 0.5 h / 35 °C
2.2: Cooling with acetone-dry ice
3.1: hydrogenchloride / ethanol; 1,4-dioxane / 2 h / 20 °C
4.1: triethylamine / dichloromethane / 18 h / 20 °C
With hydrogenchloride; titanium(IV) tetraethanolate; iodine; magnesium; triethylamine; In 2-methyltetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; 2.1: |Grignard Reaction / 2.2: |Grignard Reaction;
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