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[3-(1-{4-[2,4-dichloro-3-(2,4-dimethyl-quinolin-8-yloxymethyl)-benzenesulfonylamino]-tetrahydro-pyran-4-carbonyl}-piperidin-4-yl)-propyl]-trimethyl-ammonium trilfuoroacetate salt

Base Information Edit
  • Chemical Name:[3-(1-{4-[2,4-dichloro-3-(2,4-dimethyl-quinolin-8-yloxymethyl)-benzenesulfonylamino]-tetrahydro-pyran-4-carbonyl}-piperidin-4-yl)-propyl]-trimethyl-ammonium trilfuoroacetate salt
  • CAS No.:1369390-39-5
  • Molecular Formula:C2F3O2*C35H47Cl2N4O5S
  • Molecular Weight:819.77
  • Hs Code.:
  • Mol file:1369390-39-5.mol
[3-(1-{4-[2,4-dichloro-3-(2,4-dimethyl-quinolin-8-yloxymethyl)-benzenesulfonylamino]-tetrahydro-pyran-4-carbonyl}-piperidin-4-yl)-propyl]-trimethyl-ammonium trilfuoroacetate salt

Synonyms:[3-(1-{4-[2,4-dichloro-3-(2,4-dimethyl-quinolin-8-yloxymethyl)-benzenesulfonylamino]-tetrahydro-pyran-4-carbonyl}-piperidin-4-yl)-propyl]-trimethyl-ammonium trilfuoroacetate salt

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Chemical Property of [3-(1-{4-[2,4-dichloro-3-(2,4-dimethyl-quinolin-8-yloxymethyl)-benzenesulfonylamino]-tetrahydro-pyran-4-carbonyl}-piperidin-4-yl)-propyl]-trimethyl-ammonium trilfuoroacetate salt Edit
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Technology Process of [3-(1-{4-[2,4-dichloro-3-(2,4-dimethyl-quinolin-8-yloxymethyl)-benzenesulfonylamino]-tetrahydro-pyran-4-carbonyl}-piperidin-4-yl)-propyl]-trimethyl-ammonium trilfuoroacetate salt

There total 4 articles about [3-(1-{4-[2,4-dichloro-3-(2,4-dimethyl-quinolin-8-yloxymethyl)-benzenesulfonylamino]-tetrahydro-pyran-4-carbonyl}-piperidin-4-yl)-propyl]-trimethyl-ammonium trilfuoroacetate salt 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:
4-[2,4-dichloro-3-(2,4-dimethyl-quinolin-8-yloxymethyl)-benzenesulfonylamino]-tetrahydropyran-4-carboxylic acid; With 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; for 0.5h; Cooling with ice;
C11H25N2(1+); With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 0 - 20 ℃;
trifluoroacetic acid; In water;
DOI:10.1016/j.bmc.2012.01.036
Guidance literature:
Multi-step reaction with 3 steps
1.1: triethylamine / ethanol; N,N-dimethyl-formamide / 48 h / 80 °C
2.1: hydrogenchloride / 1,4-dioxane; methanol / 20 °C
3.1: 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0.5 h / Cooling with ice
3.2: 0 - 20 °C
With hydrogenchloride; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In 1,4-dioxane; methanol; ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2012.01.036
Guidance literature:
Multi-step reaction with 2 steps
1.1: hydrogenchloride / 1,4-dioxane; methanol / 20 °C
2.1: 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0.5 h / Cooling with ice
2.2: 0 - 20 °C
With hydrogenchloride; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,4-dioxane; methanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2012.01.036
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