2-(2-(4-(benzo[d]thiazol-2-ylmethyl)piperazin-1-yl)phenoxy)ethyl 4-methyl-benzenesulfonate

Base Information

Chemical Name:2-(2-(4-(benzo[d]thiazol-2-ylmethyl)piperazin-1-yl)phenoxy)ethyl 4-methyl-benzenesulfonate
CAS No.:1351411-93-2
Molecular Formula:C₂₇H₂₉N₃O₄S₂
Molecular Weight:523.677
Hs Code.:

Synonyms:2-(2-(4-(benzo[d]thiazol-2-ylmethyl)piperazin-1-yl)phenoxy)ethyl 4-methyl-benzenesulfonate

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Chemical Property of 2-(2-(4-(benzo[d]thiazol-2-ylmethyl)piperazin-1-yl)phenoxy)ethyl 4-methyl-benzenesulfonate

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Technology Process of 2-(2-(4-(benzo[d]thiazol-2-ylmethyl)piperazin-1-yl)phenoxy)ethyl 4-methyl-benzenesulfonate

There total 5 articles about 2-(2-(4-(benzo[d]thiazol-2-ylmethyl)piperazin-1-yl)phenoxy)ethyl 4-methyl-benzenesulfonate 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: 38.0%

: 1351411-92-1
2-(2-(4-(benzo[d]thiazol-2-ylmethyl)piperazin-1-yl)phenoxy)ethanol

: 98-59-9
p-toluenesulfonyl chloride

: 1351411-93-2
2-(2-(4-(benzo[d]thiazol-2-ylmethyl)piperazin-1-yl)phenoxy)ethyl 4-methyl-benzenesulfonate

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; for 18h;

Reference yield:

: 106086-78-6
2-(bromomethyl)-1,3-benzothiazole

: 1351411-93-2
2-(2-(4-(benzo[d]thiazol-2-ylmethyl)piperazin-1-yl)phenoxy)ethyl 4-methyl-benzenesulfonate

Guidance literature:: Multi-step reaction with 4 steps

1: N-ethyl-N,N-diisopropylamine / acetonitrile / 0.33 h / 50 °C / Microwave irradiation

2: triethylamine; caesium carbonate / acetonitrile / 18 h / 60 °C

3: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.17 h

4: triethylamine / dichloromethane / 18 h / 0 - 20 °C

With tetrabutyl ammonium fluoride; caesium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; acetonitrile;

Reference yield:

: 1011-17-2
2-hydroxyphenylpiperazine

: 1351411-93-2
2-(2-(4-(benzo[d]thiazol-2-ylmethyl)piperazin-1-yl)phenoxy)ethyl 4-methyl-benzenesulfonate

Guidance literature:: Multi-step reaction with 4 steps

1: N-ethyl-N,N-diisopropylamine / acetonitrile / 0.33 h / 50 °C / Microwave irradiation

2: triethylamine; caesium carbonate / acetonitrile / 18 h / 60 °C

3: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.17 h

4: triethylamine / dichloromethane / 18 h / 0 - 20 °C

With tetrabutyl ammonium fluoride; caesium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; acetonitrile;