tert-butyl (5-(((3S)-4-(4-(ethylsulfonyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinyl)sulfonyl)-2-pyridinyl)carbamate

Base Information

Chemical Name:tert-butyl (5-(((3S)-4-(4-(ethylsulfonyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinyl)sulfonyl)-2-pyridinyl)carbamate
CAS No.:1572928-32-5
Molecular Formula:C₂₅H₃₂N₄O₆S₂
Molecular Weight:548.684
Hs Code.:

Synonyms:tert-butyl (5-(((3S)-4-(4-(ethylsulfonyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinyl)sulfonyl)-2-pyridinyl)carbamate

Suppliers and Price of tert-butyl (5-(((3S)-4-(4-(ethylsulfonyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinyl)sulfonyl)-2-pyridinyl)carbamate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of tert-butyl (5-(((3S)-4-(4-(ethylsulfonyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinyl)sulfonyl)-2-pyridinyl)carbamate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tert-butyl (5-(((3S)-4-(4-(ethylsulfonyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinyl)sulfonyl)-2-pyridinyl)carbamate

There total 10 articles about tert-butyl (5-(((3S)-4-(4-(ethylsulfonyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinyl)sulfonyl)-2-pyridinyl)carbamate 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:

: 1450620-16-2
tert-butyl (5-(chlorosulfonyl)-2-pyridinyl)carbamate

: 1572928-31-4
(2S)-1-(4-(ethylsulfonyl)phenyl)-2-(1-propyn-1-yl)piperazine

: 1572928-32-5
tert-butyl (5-(((3S)-4-(4-(ethylsulfonyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinyl)sulfonyl)-2-pyridinyl)carbamate

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 1h; Inert atmosphere;

Reference yield:

: 1572928-30-3
(2S)-4-benzyl-1-(4-(ethylsulfonyl)phenyl)-2-(1-propyn-1-yl)piperazine

: 1572928-32-5
tert-butyl (5-(((3S)-4-(4-(ethylsulfonyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinyl)sulfonyl)-2-pyridinyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium carbonate; carbonochloridic acid 1-chloro-ethyl ester / dichloromethane / 12 h / 0 - 20 °C

1.2: 2 h / 80 °C

2.1: triethylamine / dichloromethane / 1 h / 20 °C / Inert atmosphere

With carbonochloridic acid 1-chloro-ethyl ester; potassium carbonate; triethylamine; In dichloromethane;

Reference yield:

: 1450621-78-9
(3S)-1-benzyl-3-(2-propyn-1-yl)-2,5-piperazinedione

: 1572928-32-5
tert-butyl (5-(((3S)-4-(4-(ethylsulfonyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinyl)sulfonyl)-2-pyridinyl)carbamate

Guidance literature:: Multi-step reaction with 5 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 12 h / 80 °C

2.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 20 °C

3.1: 2′-(diphenylphosphino)-N,N′-dimethyl-(1,1′-biphenyl)-2-amine; sodium t-butanolate; tris-(dibenzylideneacetone)dipalladium(0) / 1,4-dioxane / 12 h / 20 - 100 °C / Inert atmosphere

4.1: potassium carbonate; carbonochloridic acid 1-chloro-ethyl ester / dichloromethane / 12 h / 0 - 20 °C

4.2: 2 h / 80 °C

5.1: triethylamine / dichloromethane / 1 h / 20 °C / Inert atmosphere

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; lithium aluminium tetrahydride; carbonochloridic acid 1-chloro-ethyl ester; potassium tert-butylate; potassium carbonate; triethylamine; sodium t-butanolate; 2′-(diphenylphosphino)-N,N′-dimethyl-(1,1′-biphenyl)-2-amine; In tetrahydrofuran; 1,4-dioxane; dichloromethane;