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N2-(4-cyclopropyl-2-fluoro-5-(5-isopropyl-1H-tetrazol-1-yl)phenyl)-5-fluoro-N4-(2,2,6,6-tetramethylpiperidin-4-yl)pyrimidine-2,4-diamine

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  • Chemical Name:N2-(4-cyclopropyl-2-fluoro-5-(5-isopropyl-1H-tetrazol-1-yl)phenyl)-5-fluoro-N4-(2,2,6,6-tetramethylpiperidin-4-yl)pyrimidine-2,4-diamine
  • CAS No.:1356493-43-0
  • Molecular Formula:C26H35F2N9
  • Molecular Weight:511.621
  • Hs Code.:
N<sub>2</sub>-(4-cyclopropyl-2-fluoro-5-(5-isopropyl-1H-tetrazol-1-yl)phenyl)-5-fluoro-N<sub>4</sub>-(2,2,6,6-tetramethylpiperidin-4-yl)pyrimidine-2,4-diamine

Synonyms:N2-(4-cyclopropyl-2-fluoro-5-(5-isopropyl-1H-tetrazol-1-yl)phenyl)-5-fluoro-N4-(2,2,6,6-tetramethylpiperidin-4-yl)pyrimidine-2,4-diamine

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Chemical Property of N2-(4-cyclopropyl-2-fluoro-5-(5-isopropyl-1H-tetrazol-1-yl)phenyl)-5-fluoro-N4-(2,2,6,6-tetramethylpiperidin-4-yl)pyrimidine-2,4-diamine
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Technology Process of N2-(4-cyclopropyl-2-fluoro-5-(5-isopropyl-1H-tetrazol-1-yl)phenyl)-5-fluoro-N4-(2,2,6,6-tetramethylpiperidin-4-yl)pyrimidine-2,4-diamine

There total 7 articles about N2-(4-cyclopropyl-2-fluoro-5-(5-isopropyl-1H-tetrazol-1-yl)phenyl)-5-fluoro-N4-(2,2,6,6-tetramethylpiperidin-4-yl)pyrimidine-2,4-diamine 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:
2-chloro-5-fluoro-N4-(2,2,6,6-tetramethylpiperidin-4-yl)-4-pyrimidineamine hydrochloride; 4-cyclopropyl-2-fluoro-5-(5-isopropyl-1H-tetrazol-1-yl)benzenamine; With toluene-4-sulfonic acid; In isopropyl alcohol; at 70 ℃; for 168h;
With sodium hydroxide; In water; ethyl acetate; at 20 ℃;
Guidance literature:
Multi-step reaction with 6 steps
1.1: sulfuric acid / ethyl acetate / -30 - -20 °C
1.2: 1.08 h / -20 - -15 °C
2.1: tricyclohexylphosphine; caesium carbonate / palladium diacetate / toluene; water / 100 °C / Inert atmosphere
3.1: sodium hydrogencarbonate / dichloromethane / 20 °C
3.2: Cooling with ice
4.1: trifluoromethylsulfonic anhydride; trimethylsilylazide / acetonitrile / -5 °C / Inert atmosphere
5.1: hydrogen; acetic acid / palladium 10% on activated carbon / ethanol; water / 1551.49 Torr
6.1: toluene-4-sulfonic acid / isopropyl alcohol / 168 h / 70 °C
6.2: 20 °C
With trifluoromethylsulfonic anhydride; trimethylsilylazide; sulfuric acid; hydrogen; sodium hydrogencarbonate; caesium carbonate; toluene-4-sulfonic acid; acetic acid; tricyclohexylphosphine; palladium 10% on activated carbon; palladium diacetate; In ethanol; dichloromethane; water; ethyl acetate; isopropyl alcohol; toluene; acetonitrile;
Guidance literature:
Multi-step reaction with 5 steps
1.1: tricyclohexylphosphine; caesium carbonate / palladium diacetate / toluene; water / 100 °C / Inert atmosphere
2.1: sodium hydrogencarbonate / dichloromethane / 20 °C
2.2: Cooling with ice
3.1: trifluoromethylsulfonic anhydride; trimethylsilylazide / acetonitrile / -5 °C / Inert atmosphere
4.1: hydrogen; acetic acid / palladium 10% on activated carbon / ethanol; water / 1551.49 Torr
5.1: toluene-4-sulfonic acid / isopropyl alcohol / 168 h / 70 °C
5.2: 20 °C
With trifluoromethylsulfonic anhydride; trimethylsilylazide; hydrogen; sodium hydrogencarbonate; caesium carbonate; toluene-4-sulfonic acid; acetic acid; tricyclohexylphosphine; palladium 10% on activated carbon; palladium diacetate; In ethanol; dichloromethane; water; isopropyl alcohol; toluene; acetonitrile;
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