N-[4-hydroxy-3-(2-methoxyphenyl)-2-thiazolidinylidene]phenylsulfonamide

Base Information

Chemical Name:N-[4-hydroxy-3-(2-methoxyphenyl)-2-thiazolidinylidene]phenylsulfonamide
CAS No.:247031-61-4
Molecular Formula:C₁₆H₁₆N₂O₄S₂
Molecular Weight:364.446
Hs Code.:

Synonyms:N-[4-hydroxy-3-(2-methoxyphenyl)-2-thiazolidinylidene]phenylsulfonamide

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Chemical Property of N-[4-hydroxy-3-(2-methoxyphenyl)-2-thiazolidinylidene]phenylsulfonamide

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Technology Process of N-[4-hydroxy-3-(2-methoxyphenyl)-2-thiazolidinylidene]phenylsulfonamide

There total 4 articles about N-[4-hydroxy-3-(2-methoxyphenyl)-2-thiazolidinylidene]phenylsulfonamide 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: 52.0%

: 107-20-0
2-chloroethanal

: 70318-85-3
N-[[(2-methoxyphenyl)amino]thioxomethyl]phenylsulfonamide

: 247031-61-4
N-[4-hydroxy-3-(2-methoxyphenyl)-2-thiazolidinylidene]phenylsulfonamide

Guidance literature:: With potassium carbonate; In water; acetone; for 2.5h; Heating;
DOI:10.1016/S0223-5234(99)80082-8

Reference yield:

: 98-10-2
benzenesulfonamide

: 247031-61-4
N-[4-hydroxy-3-(2-methoxyphenyl)-2-thiazolidinylidene]phenylsulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: aq. NaOH / dimethylformamide

2: dimethylformamide / 2 h / 20 °C

3: 70 percent / tetrahydrofuran / 20 h / Heating

4: 52 percent / K₂CO₃ / acetone; H₂O / 2.5 h / Heating

With sodium hydroxide; potassium carbonate; In tetrahydrofuran; water; N,N-dimethyl-formamide; acetone; 1: Addition / 2: Methylation / 3: Substitution / 4: Cyclization;
DOI:10.1016/S0223-5234(99)80082-8

Reference yield:

: 20902-00-5
N-Benzensulfonyldithiocarbamidsaeuremethylester

: 247031-61-4
N-[4-hydroxy-3-(2-methoxyphenyl)-2-thiazolidinylidene]phenylsulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / tetrahydrofuran / 20 h / Heating

2: 52 percent / K₂CO₃ / acetone; H₂O / 2.5 h / Heating

With potassium carbonate; In tetrahydrofuran; water; acetone; 1: Substitution / 2: Cyclization;
DOI:10.1016/S0223-5234(99)80082-8