5-{4-[2-(4-Methyl-piperazin-1-yl)-ethoxy]-benzyl}-thiazolidine-2,4-dione; hydrochloride

Base Information

Chemical Name:5-{4-[2-(4-Methyl-piperazin-1-yl)-ethoxy]-benzyl}-thiazolidine-2,4-dione; hydrochloride
CAS No.:85002-34-2
Molecular Formula:C₁₇H₂₃N₃O₃S*2ClH
Molecular Weight:422.376
Hs Code.:

Synonyms:5-{4-[2-(4-Methyl-piperazin-1-yl)-ethoxy]-benzyl}-thiazolidine-2,4-dione; hydrochloride

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Chemical Property of 5-{4-[2-(4-Methyl-piperazin-1-yl)-ethoxy]-benzyl}-thiazolidine-2,4-dione; hydrochloride

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Technology Process of 5-{4-[2-(4-Methyl-piperazin-1-yl)-ethoxy]-benzyl}-thiazolidine-2,4-dione; hydrochloride

There total 5 articles about 5-{4-[2-(4-Methyl-piperazin-1-yl)-ethoxy]-benzyl}-thiazolidine-2,4-dione; hydrochloride 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:

: 100-00-5
4-chlorobenzonitrile

: 85002-34-2
5-{4-[2-(4-Methyl-piperazin-1-yl)-ethoxy]-benzyl}-thiazolidine-2,4-dione; hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1: 69.1 percent / NaH / dimethylsulfoxide / 0.5 h / 70 °C

2: hydrogen / 10percent Pd-C / methanol / 760 Torr / Ambient temperature

3: 1.) NaNO₂, conc. HCl, 2.) Cu₂O / 1.) acetone, water, 5 deg C, 30 min, 2.) acetone, water, 35 deg C

4: 2.) 2N HCl / 1.) sulfolane, 120 deg C, 10 h; 2.) sulfolane, 100 deg C, 8 h

With copper(I) oxide; hydrogenchloride; hydrogen; sodium hydride; sodium nitrite; palladium on activated charcoal; In methanol; dimethyl sulfoxide;
DOI:10.1248/cpb.30.3580

Reference yield:

: 5464-12-0
2-(4-methylpiperazinyl)ethanol

: 85002-34-2
5-{4-[2-(4-Methyl-piperazin-1-yl)-ethoxy]-benzyl}-thiazolidine-2,4-dione; hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1: 69.1 percent / NaH / dimethylsulfoxide / 0.5 h / 70 °C

2: hydrogen / 10percent Pd-C / methanol / 760 Torr / Ambient temperature

3: 1.) NaNO₂, conc. HCl, 2.) Cu₂O / 1.) acetone, water, 5 deg C, 30 min, 2.) acetone, water, 35 deg C

4: 2.) 2N HCl / 1.) sulfolane, 120 deg C, 10 h; 2.) sulfolane, 100 deg C, 8 h

With copper(I) oxide; hydrogenchloride; hydrogen; sodium hydride; sodium nitrite; palladium on activated charcoal; In methanol; dimethyl sulfoxide;
DOI:10.1248/cpb.30.3580

Reference yield:

: 85002-95-5
1-Methyl-4-[2-(4-nitro-phenoxy)-ethyl]-piperazine; hydrochloride

: 85002-34-2
5-{4-[2-(4-Methyl-piperazin-1-yl)-ethoxy]-benzyl}-thiazolidine-2,4-dione; hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogen / 10percent Pd-C / methanol / 760 Torr / Ambient temperature

2: 1.) NaNO₂, conc. HCl, 2.) Cu₂O / 1.) acetone, water, 5 deg C, 30 min, 2.) acetone, water, 35 deg C

3: 2.) 2N HCl / 1.) sulfolane, 120 deg C, 10 h; 2.) sulfolane, 100 deg C, 8 h

With copper(I) oxide; hydrogenchloride; hydrogen; sodium nitrite; palladium on activated charcoal; In methanol;
DOI:10.1248/cpb.30.3580