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2,2,2-trifluoroethanesulfonic acid ((1R,2R)-2-{5-chloro-2-[3-(2-methoxyethyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ylamino]pyrimidin-4-ylamino}cyclohexyl)amide

Base Information
  • Chemical Name:2,2,2-trifluoroethanesulfonic acid ((1R,2R)-2-{5-chloro-2-[3-(2-methoxyethyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ylamino]pyrimidin-4-ylamino}cyclohexyl)amide
  • CAS No.:1022973-46-1
  • Molecular Formula:C25H34ClF3N6O3S
  • Molecular Weight:591.098
  • Hs Code.:
2,2,2-trifluoroethanesulfonic acid ((1R,2R)-2-{5-chloro-2-[3-(2-methoxyethyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ylamino]pyrimidin-4-ylamino}cyclohexyl)amide

Synonyms:2,2,2-trifluoroethanesulfonic acid ((1R,2R)-2-{5-chloro-2-[3-(2-methoxyethyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ylamino]pyrimidin-4-ylamino}cyclohexyl)amide

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Chemical Property of 2,2,2-trifluoroethanesulfonic acid ((1R,2R)-2-{5-chloro-2-[3-(2-methoxyethyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ylamino]pyrimidin-4-ylamino}cyclohexyl)amide
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Technology Process of 2,2,2-trifluoroethanesulfonic acid ((1R,2R)-2-{5-chloro-2-[3-(2-methoxyethyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ylamino]pyrimidin-4-ylamino}cyclohexyl)amide

There total 5 articles about 2,2,2-trifluoroethanesulfonic acid ((1R,2R)-2-{5-chloro-2-[3-(2-methoxyethyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ylamino]pyrimidin-4-ylamino}cyclohexyl)amide 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 4 steps
1: triethylamine / tetrahydrofuran / 0.25 h / 0 °C
2: hydrogenchloride / 1,4-dioxane; ethyl methyl ether / 120 °C
3: water; potassium hydroxide / methanol / 7 h / 60 °C
4: triethylamine / dichloromethane / 0.75 h / 20 °C / Inert atmosphere
With hydrogenchloride; water; triethylamine; potassium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; ethyl methyl ether; dichloromethane;
DOI:10.1016/j.bmcl.2011.05.040
Guidance literature:
Multi-step reaction with 2 steps
1: water; potassium hydroxide / methanol / 7 h / 60 °C
2: triethylamine / dichloromethane / 0.75 h / 20 °C / Inert atmosphere
With water; triethylamine; potassium hydroxide; In methanol; dichloromethane;
DOI:10.1016/j.bmcl.2011.05.040
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