1-(tert-butoxycarbonyl)-4-[(5-chloro-1-phenylsulfonylindol-2-yl)sulfonyl]piperazine

Base Information

Chemical Name:1-(tert-butoxycarbonyl)-4-[(5-chloro-1-phenylsulfonylindol-2-yl)sulfonyl]piperazine
CAS No.:259807-33-5
Molecular Formula:C₂₃H₂₆ClN₃O₆S₂
Molecular Weight:540.061
Hs Code.:

Synonyms:1-(tert-butoxycarbonyl)-4-[(5-chloro-1-phenylsulfonylindol-2-yl)sulfonyl]piperazine

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Chemical Property of 1-(tert-butoxycarbonyl)-4-[(5-chloro-1-phenylsulfonylindol-2-yl)sulfonyl]piperazine

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Technology Process of 1-(tert-butoxycarbonyl)-4-[(5-chloro-1-phenylsulfonylindol-2-yl)sulfonyl]piperazine

There total 3 articles about 1-(tert-butoxycarbonyl)-4-[(5-chloro-1-phenylsulfonylindol-2-yl)sulfonyl]piperazine 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:

: 17422-32-1
5-chloro-1H-indole

: 259807-33-5
1-(tert-butoxycarbonyl)-4-[(5-chloro-1-phenylsulfonylindol-2-yl)sulfonyl]piperazine

Guidance literature:: Multi-step reaction with 3 steps

1.1: 93 percent / n-butyl lithium / tetrahydrofuran; hexane / -78 - 20 °C

2.1: tert-butyl lithium / diethyl ether; pentane / -78 - -40 °C

2.2: SO₂ / diethyl ether; pentane / -78 - 20 °C

2.3: 64 percent / N-chlorosuccinimide / CH₂Cl₂ / 8 h / 20 °C

3.1: 3.63 g / triethylamine / CH₂Cl₂ / 3 h / 20 °C

With n-butyllithium; tert.-butyl lithium; triethylamine; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; pentane;
DOI:10.1016/j.bmc.2005.04.006

Reference yield:

: 78329-47-2
5-chloro-1-(phenylsulfonyl)-1H-indole

: 259807-33-5
1-(tert-butoxycarbonyl)-4-[(5-chloro-1-phenylsulfonylindol-2-yl)sulfonyl]piperazine

Guidance literature:: Multi-step reaction with 2 steps

1.1: tert-butyl lithium / diethyl ether; pentane / -78 - -40 °C

1.2: SO₂ / diethyl ether; pentane / -78 - 20 °C

1.3: 64 percent / N-chlorosuccinimide / CH₂Cl₂ / 8 h / 20 °C

2.1: 3.63 g / triethylamine / CH₂Cl₂ / 3 h / 20 °C

With tert.-butyl lithium; triethylamine; In diethyl ether; dichloromethane; pentane;
DOI:10.1016/j.bmc.2005.04.006

Reference yield:

: 98-09-9
benzenesulfonyl chloride

: 259807-33-5
1-(tert-butoxycarbonyl)-4-[(5-chloro-1-phenylsulfonylindol-2-yl)sulfonyl]piperazine

Guidance literature:: Multi-step reaction with 3 steps

1.1: 93 percent / n-butyl lithium / tetrahydrofuran; hexane / -78 - 20 °C

2.1: tert-butyl lithium / diethyl ether; pentane / -78 - -40 °C

2.2: SO₂ / diethyl ether; pentane / -78 - 20 °C

2.3: 64 percent / N-chlorosuccinimide / CH₂Cl₂ / 8 h / 20 °C

3.1: 3.63 g / triethylamine / CH₂Cl₂ / 3 h / 20 °C

With n-butyllithium; tert.-butyl lithium; triethylamine; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; pentane;
DOI:10.1016/j.bmc.2005.04.006