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N-[5-[4-(5-{[(2R,6S)-2,6-dimethyl-4-morpholinyl]methyl}-1,3-oxazol-2-yl)-1H-indazol-6-yl]-2-(methyloxy)-3-pyridinyl]methanesulfonamide tosylate salt

Base Information
  • Chemical Name:N-[5-[4-(5-{[(2R,6S)-2,6-dimethyl-4-morpholinyl]methyl}-1,3-oxazol-2-yl)-1H-indazol-6-yl]-2-(methyloxy)-3-pyridinyl]methanesulfonamide tosylate salt
  • CAS No.:1361970-34-4
  • Molecular Formula:C7H8O3S*C24H28N6O5S
  • Molecular Weight:684.794
  • Hs Code.:
N-[5-[4-(5-{[(2R,6S)-2,6-dimethyl-4-morpholinyl]methyl}-1,3-oxazol-2-yl)-1H-indazol-6-yl]-2-(methyloxy)-3-pyridinyl]methanesulfonamide tosylate salt

Synonyms:N-[5-[4-(5-{[(2R,6S)-2,6-dimethyl-4-morpholinyl]methyl}-1,3-oxazol-2-yl)-1H-indazol-6-yl]-2-(methyloxy)-3-pyridinyl]methanesulfonamide tosylate salt

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Chemical Property of N-[5-[4-(5-{[(2R,6S)-2,6-dimethyl-4-morpholinyl]methyl}-1,3-oxazol-2-yl)-1H-indazol-6-yl]-2-(methyloxy)-3-pyridinyl]methanesulfonamide tosylate salt
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Technology Process of N-[5-[4-(5-{[(2R,6S)-2,6-dimethyl-4-morpholinyl]methyl}-1,3-oxazol-2-yl)-1H-indazol-6-yl]-2-(methyloxy)-3-pyridinyl]methanesulfonamide tosylate salt

There total 17 articles about N-[5-[4-(5-{[(2R,6S)-2,6-dimethyl-4-morpholinyl]methyl}-1,3-oxazol-2-yl)-1H-indazol-6-yl]-2-(methyloxy)-3-pyridinyl]methanesulfonamide tosylate 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:
Multi-step reaction with 7 steps
1.1: methanol / 2.75 h / 0 - 10 °C / Industry scale; Inert atmosphere
2.1: hydrogenchloride; iron / ethanol; water / 23 h / 10 - 25 °C / Industry scale; Inert atmosphere
3.1: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / 1,4-dioxane / 2 h / 80 °C / Inert atmosphere
4.1: pyridine / 18 h / 20 °C
5.1: potassium phosphate; potassium hydrogenfluoride / tricyclohexylphosphine; palladium diacetate / isopropyl alcohol; water / 2 h / 75 - 80 °C / Inert atmosphere
6.1: sodium hydroxide; water / 3.08 h / 17 - 23 °C
6.2: 30 °C / pH 6.6
7.1: tetrahydrofuran / 20 °C
With pyridine; hydrogenchloride; potassium phosphate; potassium hydrogenfluoride; water; potassium acetate; iron; sodium hydroxide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; palladium diacetate; tricyclohexylphosphine; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; water; isopropyl alcohol;
Guidance literature:
Multi-step reaction with 6 steps
1.1: hydrogenchloride; iron / ethanol; water / 23 h / 10 - 25 °C / Industry scale; Inert atmosphere
2.1: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / 1,4-dioxane / 2 h / 80 °C / Inert atmosphere
3.1: pyridine / 18 h / 20 °C
4.1: potassium phosphate; potassium hydrogenfluoride / tricyclohexylphosphine; palladium diacetate / isopropyl alcohol; water / 2 h / 75 - 80 °C / Inert atmosphere
5.1: sodium hydroxide; water / 3.08 h / 17 - 23 °C
5.2: 30 °C / pH 6.6
6.1: tetrahydrofuran / 20 °C
With pyridine; hydrogenchloride; potassium phosphate; potassium hydrogenfluoride; water; potassium acetate; iron; sodium hydroxide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; palladium diacetate; tricyclohexylphosphine; In tetrahydrofuran; 1,4-dioxane; ethanol; water; isopropyl alcohol;
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