N-(3,4-Dimethyl-5-isoxazolyl)-2-[1-(phenylsulfonyl)-1H-indol-3-yl]benzenesulfonamide

Base Information

Chemical Name:N-(3,4-Dimethyl-5-isoxazolyl)-2-[1-(phenylsulfonyl)-1H-indol-3-yl]benzenesulfonamide
CAS No.:236096-42-7
Molecular Formula:C₂₅H₂₁N₃O₅S₂
Molecular Weight:507.591
Hs Code.:

Synonyms:N-(3,4-Dimethyl-5-isoxazolyl)-2-[1-(phenylsulfonyl)-1H-indol-3-yl]benzenesulfonamide

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Chemical Property of N-(3,4-Dimethyl-5-isoxazolyl)-2-[1-(phenylsulfonyl)-1H-indol-3-yl]benzenesulfonamide

Chemical Property:

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Technology Process of N-(3,4-Dimethyl-5-isoxazolyl)-2-[1-(phenylsulfonyl)-1H-indol-3-yl]benzenesulfonamide

There total 6 articles about N-(3,4-Dimethyl-5-isoxazolyl)-2-[1-(phenylsulfonyl)-1H-indol-3-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:

: 236096-48-3
N-(3,4-Dimethyl-5-isoxazolyl)-N-[(2-methoxyethoxy)methyl]-2-[1-(phenylsulfonyl)-1H-indol-3-yl]benzenesulfonamide

: 236096-42-7
N-(3,4-Dimethyl-5-isoxazolyl)-2-[1-(phenylsulfonyl)-1H-indol-3-yl]benzenesulfonamide

Guidance literature:: With hydrogenchloride; In ethanol; for 2h; Heating;
DOI:10.1021/jm970872k

Reference yield:

: 19947-75-2
5-amino-3,4-dimethylisoxazol

: 236096-42-7
N-(3,4-Dimethyl-5-isoxazolyl)-2-[1-(phenylsulfonyl)-1H-indol-3-yl]benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: 90 percent / pyridine / Ambient temperature

2: 1.) NaH / 1.) THF, RT, 10 min, 2.) THF, RT, overnight

3: (Ph₃P)4Pd, aq. Na₂CO₃ / ethanol; benzene / 10 h / Heating

4: 6 N aq. HCl / aq. ethanol / 2 h / Heating

With pyridine; hydrogenchloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium hydride; sodium carbonate; In ethanol; benzene;
DOI:10.1021/jm970872k

Reference yield:

: 2905-25-1
o-bromobenzenesulfonyl chloride

: 236096-42-7
N-(3,4-Dimethyl-5-isoxazolyl)-2-[1-(phenylsulfonyl)-1H-indol-3-yl]benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: 90 percent / pyridine / Ambient temperature

2: 1.) NaH / 1.) THF, RT, 10 min, 2.) THF, RT, overnight

3: (Ph₃P)4Pd, aq. Na₂CO₃ / ethanol; benzene / 10 h / Heating

4: 6 N aq. HCl / aq. ethanol / 2 h / Heating

With pyridine; hydrogenchloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium hydride; sodium carbonate; In ethanol; benzene;
DOI:10.1021/jm970872k