N-(3-(3-sulfamoylphenyl)-1H-indazol-5-yl)-2,3-dihydro-1H-indene-1-carboxamide

Base Information

Chemical Name:N-(3-(3-sulfamoylphenyl)-1H-indazol-5-yl)-2,3-dihydro-1H-indene-1-carboxamide
CAS No.:1338792-55-4
Molecular Formula:C₂₃H₂₀N₄O₃S
Molecular Weight:432.503
Hs Code.:

Synonyms:N-(3-(3-sulfamoylphenyl)-1H-indazol-5-yl)-2,3-dihydro-1H-indene-1-carboxamide

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Chemical Property of N-(3-(3-sulfamoylphenyl)-1H-indazol-5-yl)-2,3-dihydro-1H-indene-1-carboxamide

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Technology Process of N-(3-(3-sulfamoylphenyl)-1H-indazol-5-yl)-2,3-dihydro-1H-indene-1-carboxamide

There total 6 articles about N-(3-(3-sulfamoylphenyl)-1H-indazol-5-yl)-2,3-dihydro-1H-indene-1-carboxamide 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: 70.0%

: 1338792-54-3
N-(3-(3-sulfamoylphenyl)-1H-indazol-5-yl)-1H-indene-3-carboxamide

: 1338792-55-4
N-(3-(3-sulfamoylphenyl)-1H-indazol-5-yl)-2,3-dihydro-1H-indene-1-carboxamide

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In tetrahydrofuran; methanol; for 2h;

Reference yield:

: 19335-11-6
1H-indazol-5-ylamine

: 1338792-55-4
N-(3-(3-sulfamoylphenyl)-1H-indazol-5-yl)-2,3-dihydro-1H-indene-1-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0 - 20 °C

2: potassium carbonate; iodine / N,N-dimethyl-formamide / 3 h / 0 °C

3: potassium fluoride / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide; water / 1.5 h / 120 °C / Inert atmosphere; Sealed; Microwave irradiation

4: dichloromethane / 3 h / 0 - 20 °C

5: N-ethyl-N,N-diisopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 1 h / 0 °C

6: hydrogen / palladium 10% on activated carbon / tetrahydrofuran; methanol / 2 h

With potassium fluoride; hydrogen; iodine; potassium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 917474-59-0
(1H-indazol-5-yl)-carbamic acid tert-butyl ester

: 1338792-55-4
N-(3-(3-sulfamoylphenyl)-1H-indazol-5-yl)-2,3-dihydro-1H-indene-1-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate; iodine / N,N-dimethyl-formamide / 3 h / 0 °C

2: potassium fluoride / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide; water / 1.5 h / 120 °C / Inert atmosphere; Sealed; Microwave irradiation

3: dichloromethane / 3 h / 0 - 20 °C

4: N-ethyl-N,N-diisopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 1 h / 0 °C

5: hydrogen / palladium 10% on activated carbon / tetrahydrofuran; methanol / 2 h

With potassium fluoride; hydrogen; iodine; potassium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;