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(S)-3-[(5-chloro-thiophene-2-carbonyl)-amino]-2-[2-ethyl-3-(3-oxo-morpholin-4-yl)-benzenesulfonylamino]-propionic acid

Base Information Edit
  • Chemical Name:(S)-3-[(5-chloro-thiophene-2-carbonyl)-amino]-2-[2-ethyl-3-(3-oxo-morpholin-4-yl)-benzenesulfonylamino]-propionic acid
  • CAS No.:1184297-45-7
  • Molecular Formula:C20H22ClN3O7S2
  • Molecular Weight:515.996
  • Hs Code.:
  • Mol file:1184297-45-7.mol
(S)-3-[(5-chloro-thiophene-2-carbonyl)-amino]-2-[2-ethyl-3-(3-oxo-morpholin-4-yl)-benzenesulfonylamino]-propionic acid

Synonyms:(S)-3-[(5-chloro-thiophene-2-carbonyl)-amino]-2-[2-ethyl-3-(3-oxo-morpholin-4-yl)-benzenesulfonylamino]-propionic acid

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Chemical Property of (S)-3-[(5-chloro-thiophene-2-carbonyl)-amino]-2-[2-ethyl-3-(3-oxo-morpholin-4-yl)-benzenesulfonylamino]-propionic acid Edit
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Technology Process of (S)-3-[(5-chloro-thiophene-2-carbonyl)-amino]-2-[2-ethyl-3-(3-oxo-morpholin-4-yl)-benzenesulfonylamino]-propionic acid

There total 9 articles about (S)-3-[(5-chloro-thiophene-2-carbonyl)-amino]-2-[2-ethyl-3-(3-oxo-morpholin-4-yl)-benzenesulfonylamino]-propionic acid 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:
Guidance literature:
(S)-3-[(5-chloro-thiophene-2-carbonyl)-amino]-2-[2-ethyl-3-(3-oxo-morpholin-4-yl)-benzenesulfonylamino]-propionic acid methyl ester; With water; lithium hydroxide; In tetrahydrofuran; methanol; for 4h;
With hydrogenchloride; In water;
Guidance literature:
Multi-step reaction with 6 steps
1.1: lithium diisopropyl amide / tetrahydrofuran; n-heptane; ethylbenzene / -78 - -65 °C / Inert atmosphere
1.2: 0.33 h / Saturated solution
2.1: n-butyllithium / tetrahydrofuran; n-heptane / 0.25 h / -78 °C
2.2: 0.5 h / -78 °C / Inert atmosphere
2.3: 1.5 h / -78 °C
3.1: potassium carbonate / copper(l) iodide; N,N`-dimethylethylenediamine / toluene / 20 h / 110 °C / Inert atmosphere
4.1: sulfuryl dichloride; water; acetic acid / dichloromethane / 1.58 h / 0 - 20 °C
5.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C
6.1: water; lithium hydroxide / tetrahydrofuran; methanol / 4 h
With n-butyllithium; sulfuryl dichloride; water; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; lithium hydroxide; lithium diisopropyl amide; copper(l) iodide; N,N`-dimethylethylenediamine; In tetrahydrofuran; methanol; n-heptane; dichloromethane; ethylbenzene; toluene;
Guidance literature:
Multi-step reaction with 5 steps
1.1: n-butyllithium / tetrahydrofuran; n-heptane / 0.25 h / -78 °C
1.2: 0.5 h / -78 °C / Inert atmosphere
1.3: 1.5 h / -78 °C
2.1: potassium carbonate / copper(l) iodide; N,N`-dimethylethylenediamine / toluene / 20 h / 110 °C / Inert atmosphere
3.1: sulfuryl dichloride; water; acetic acid / dichloromethane / 1.58 h / 0 - 20 °C
4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C
5.1: water; lithium hydroxide / tetrahydrofuran; methanol / 4 h
With n-butyllithium; sulfuryl dichloride; water; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; lithium hydroxide; copper(l) iodide; N,N`-dimethylethylenediamine; In tetrahydrofuran; methanol; n-heptane; dichloromethane; toluene;
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