N-{3-[1-(4-chloro-2-fluorophenyl)-3-cyanopropyl]-1H-indazol-7-yl}methanesulfonamide

Base Information

Chemical Name:N-{3-[1-(4-chloro-2-fluorophenyl)-3-cyanopropyl]-1H-indazol-7-yl}methanesulfonamide
CAS No.:1402892-61-8
Molecular Formula:C₁₈H₁₆ClFN₄O₂S
Molecular Weight:406.868
Hs Code.:

Synonyms:N-{3-[1-(4-chloro-2-fluorophenyl)-3-cyanopropyl]-1H-indazol-7-yl}methanesulfonamide

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Chemical Property of N-{3-[1-(4-chloro-2-fluorophenyl)-3-cyanopropyl]-1H-indazol-7-yl}methanesulfonamide

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Technology Process of N-{3-[1-(4-chloro-2-fluorophenyl)-3-cyanopropyl]-1H-indazol-7-yl}methanesulfonamide

There total 6 articles about N-{3-[1-(4-chloro-2-fluorophenyl)-3-cyanopropyl]-1H-indazol-7-yl}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:

Reference yield:

: 1402892-03-8
N-{3-[1-(4-chloro-2-fluorophenyl)-3-cyanopropyl]-1H-indazol-7-yl}methanesulfonamide

: 1402892-61-8
N-{3-[1-(4-chloro-2-fluorophenyl)-3-cyanopropyl]-1H-indazol-7-yl}methanesulfonamide

: 1402892-62-9
N-{3-[1-(4-chloro-2-fluorophenyl)-3-cyanopropyl]-1H-indazol-7-yl}methanesulfonamide

Guidance literature:: With carbon dioxide; In methanol; at 35 ℃; under 75007.5 Torr; Purification / work up;

Reference yield:

: 194240-75-0
2-(4-chloro-2-fluorophenyl)acetic acid

: 1402892-61-8
N-{3-[1-(4-chloro-2-fluorophenyl)-3-cyanopropyl]-1H-indazol-7-yl}methanesulfonamide

: 1402892-62-9
N-{3-[1-(4-chloro-2-fluorophenyl)-3-cyanopropyl]-1H-indazol-7-yl}methanesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hexamethyldisilazane / tetrahydrofuran / 6 h / -78 °C

1.2: 0.5 h / 20 °C

2.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.5 h / -78 °C

2.2: -78 - 20 °C

3.1: hydrazine / pyridine / 0.5 h / 120 °C

4.1: potassium phosphate; copper(l) iodide; (R,R)-N,N'-dimethyl-1,2-diaminocyclohexane / 1,4-dioxane / 110 °C / Inert atmosphere

5.1: carbon dioxide / methanol / 35 °C / 75007.5 Torr

With potassium phosphate; copper(l) iodide; carbon dioxide; (R,R)-N,N'-dimethyl-1,2-diaminocyclohexane; sodium hexamethyldisilazane; lithium hexamethyldisilazane; hydrazine; In tetrahydrofuran; 1,4-dioxane; pyridine; methanol; 1.1: Claisen Reaction;

Reference yield:

: 1402892-33-4
2-(4-chloro-2-fluorophenyl)-1-(2-fluoro-3-iodophenyl)ethanone

: 1402892-61-8
N-{3-[1-(4-chloro-2-fluorophenyl)-3-cyanopropyl]-1H-indazol-7-yl}methanesulfonamide

: 1402892-62-9
N-{3-[1-(4-chloro-2-fluorophenyl)-3-cyanopropyl]-1H-indazol-7-yl}methanesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.5 h / -78 °C

1.2: -78 - 20 °C

2.1: hydrazine / pyridine / 0.5 h / 120 °C

3.1: potassium phosphate; copper(l) iodide; (R,R)-N,N'-dimethyl-1,2-diaminocyclohexane / 1,4-dioxane / 110 °C / Inert atmosphere

4.1: carbon dioxide / methanol / 35 °C / 75007.5 Torr

With potassium phosphate; copper(l) iodide; carbon dioxide; (R,R)-N,N'-dimethyl-1,2-diaminocyclohexane; lithium hexamethyldisilazane; hydrazine; In tetrahydrofuran; 1,4-dioxane; pyridine; methanol;