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N-[7-fluoro-3,3-dimethyl-2-(3-morpholin-4-yl-phenyl)-1,2,3,4-tetrahydro-quinoline-5-carbonyl]-methanesulfonamide

Base Information Edit
  • Chemical Name:N-[7-fluoro-3,3-dimethyl-2-(3-morpholin-4-yl-phenyl)-1,2,3,4-tetrahydro-quinoline-5-carbonyl]-methanesulfonamide
  • CAS No.:1343460-31-0
  • Molecular Formula:C23H28FN3O4S
  • Molecular Weight:461.557
  • Hs Code.:
  • Mol file:1343460-31-0.mol
N-[7-fluoro-3,3-dimethyl-2-(3-morpholin-4-yl-phenyl)-1,2,3,4-tetrahydro-quinoline-5-carbonyl]-methanesulfonamide

Synonyms:N-[7-fluoro-3,3-dimethyl-2-(3-morpholin-4-yl-phenyl)-1,2,3,4-tetrahydro-quinoline-5-carbonyl]-methanesulfonamide

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Chemical Property of N-[7-fluoro-3,3-dimethyl-2-(3-morpholin-4-yl-phenyl)-1,2,3,4-tetrahydro-quinoline-5-carbonyl]-methanesulfonamide Edit
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Technology Process of N-[7-fluoro-3,3-dimethyl-2-(3-morpholin-4-yl-phenyl)-1,2,3,4-tetrahydro-quinoline-5-carbonyl]-methanesulfonamide

There total 7 articles about N-[7-fluoro-3,3-dimethyl-2-(3-morpholin-4-yl-phenyl)-1,2,3,4-tetrahydro-quinoline-5-carbonyl]-methanesulfonamide 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:
methanesulfonamide; With sodium hydride; In N,N-dimethyl-formamide; at 20 - 25 ℃; for 1h;
7-fluoro-3,3-dimethyl-2-(3-morpholin-4-yl-phenyl)-1,2,3,4-tetrahydro-quinoline-5-carboxylic acid; With 1,1'-carbonyldiimidazole; In N,N-dimethyl-formamide; at 25 ℃; for 1h;
Guidance literature:
Multi-step reaction with 7 steps
1.1: thionyl chloride / 12 h / 0 °C / Reflux
2.1: toluene-4-sulfonic acid / toluene / 12 h / Reflux
3.1: water / ytterbium(III) trifluoromethanesulfonate hydrate / tetrahydrofuran / 16 h / 25 °C
4.1: trifluoroacetic acid; triethylsilane / 3 h / 25 °C
5.1: potassium carbonate / copper(l) iodide; N,N-dimethylglycine hydrochoride / dimethyl sulfoxide / 16 h / 120 °C
6.1: sodium hydroxide; water / tetrahydrofuran; methanol / 6 h / 70 °C
7.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 20 - 25 °C
7.2: 1 h / 25 °C
With triethylsilane; thionyl chloride; water; sodium hydride; potassium carbonate; toluene-4-sulfonic acid; trifluoroacetic acid; sodium hydroxide; copper(l) iodide; ytterbium(III) trifluoromethanesulfonate hydrate; N,N-dimethylglycine hydrochoride; In tetrahydrofuran; methanol; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene; 3.1: Diels-Alder Reaction / 5.1: Ullmann Reaction;
Guidance literature:
Multi-step reaction with 4 steps
1.1: trifluoroacetic acid; triethylsilane / 3 h / 25 °C
2.1: potassium carbonate / copper(l) iodide; N,N-dimethylglycine hydrochoride / dimethyl sulfoxide / 16 h / 120 °C
3.1: sodium hydroxide; water / tetrahydrofuran; methanol / 6 h / 70 °C
4.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 20 - 25 °C
4.2: 1 h / 25 °C
With triethylsilane; water; sodium hydride; potassium carbonate; trifluoroacetic acid; sodium hydroxide; copper(l) iodide; N,N-dimethylglycine hydrochoride; In tetrahydrofuran; methanol; dimethyl sulfoxide; N,N-dimethyl-formamide; 2.1: Ullmann Reaction;
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