[5-(3-isopropyl-5-trifluoromethyl-benzenesulfonylamino)-6,7,8,9-tetrahydro-5H-benzocyclohepten-1-yloxy]-acetic acid

Base Information

Chemical Name:[5-(3-isopropyl-5-trifluoromethyl-benzenesulfonylamino)-6,7,8,9-tetrahydro-5H-benzocyclohepten-1-yloxy]-acetic acid
CAS No.:1415654-12-4
Molecular Formula:C₂₃H₂₆F₃NO₅S
Molecular Weight:485.524
Hs Code.:

Synonyms:[5-(3-isopropyl-5-trifluoromethyl-benzenesulfonylamino)-6,7,8,9-tetrahydro-5H-benzocyclohepten-1-yloxy]-acetic acid

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Chemical Property of [5-(3-isopropyl-5-trifluoromethyl-benzenesulfonylamino)-6,7,8,9-tetrahydro-5H-benzocyclohepten-1-yloxy]-acetic acid

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Technology Process of [5-(3-isopropyl-5-trifluoromethyl-benzenesulfonylamino)-6,7,8,9-tetrahydro-5H-benzocyclohepten-1-yloxy]-acetic acid

There total 3 articles about [5-(3-isopropyl-5-trifluoromethyl-benzenesulfonylamino)-6,7,8,9-tetrahydro-5H-benzocyclohepten-1-yloxy]-acetic acid 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:

Reference yield: 86.0%

: 1415654-44-2
[5-(3-isopropyl-5-trifluoromethyl-benzenesulfonylamino)-6,7,8,9-tetrahydro-5H-benzocyclohepten-1-yloxy]-acetic acid tert-butyl ester

: 1415654-12-4
[5-(3-isopropyl-5-trifluoromethyl-benzenesulfonylamino)-6,7,8,9-tetrahydro-5H-benzocyclohepten-1-yloxy]-acetic acid

Guidance literature:: [5-(3-isopropyl-5-trifluoromethyl-benzenesulfonylamino)-6,7,8,9-tetrahydro-5H-benzocyclohepten-1-yloxy]-acetic acid tert-butyl ester; With lithium hydroxide monohydrate; water; In tetrahydrofuran; methanol; for 16h;

With hydrogenchloride; In water; pH=~ 4;

Reference yield:

: 1415654-18-0
[5-(3-isopropenyl-5-trifluoromethyl-benzenesulfonylamino)-6,7,8,9-tetrahydro-5H-benzocyclohepten-1-yloxy]-acetic acid tert-butyl ester

: 1415654-12-4
[5-(3-isopropyl-5-trifluoromethyl-benzenesulfonylamino)-6,7,8,9-tetrahydro-5H-benzocyclohepten-1-yloxy]-acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogen / palladium 10% on activated carbon / methanol / 16 h / 20 °C

2.1: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 16 h

2.2: pH ~ 4

With lithium hydroxide monohydrate; water; hydrogen; palladium 10% on activated carbon; In tetrahydrofuran; methanol;

Reference yield:

: 1415654-28-2
[5-(3-bromo-5-trifluoromethyl-benzenesulfonylamino)-6,7,8,9-tetrahydro-5H-benzocyclohepten-1-yloxy]-acetic acid tert-butyl ester

: 1415654-12-4
[5-(3-isopropyl-5-trifluoromethyl-benzenesulfonylamino)-6,7,8,9-tetrahydro-5H-benzocyclohepten-1-yloxy]-acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane / 16 h / 100 °C / Inert atmosphere; Sealed tube

2.1: hydrogen / palladium 10% on activated carbon / methanol / 16 h / 20 °C

3.1: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 16 h

3.2: pH ~ 4

With lithium hydroxide monohydrate; water; hydrogen; potassium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium 10% on activated carbon; In tetrahydrofuran; 1,4-dioxane; methanol; 1.1: Suzuki Coupling;