2-((2-[bis(pyridin-2-ylmethyl)amino]ethyl)amino)-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydroindazol-1-yl)benzamide

Base Information

Chemical Name:2-((2-[bis(pyridin-2-ylmethyl)amino]ethyl)amino)-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydroindazol-1-yl)benzamide
CAS No.:1392213-63-6
Molecular Formula:C₃₁H₃₅N₇O₂
Molecular Weight:537.665
Hs Code.:

Synonyms:2-((2-[bis(pyridin-2-ylmethyl)amino]ethyl)amino)-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydroindazol-1-yl)benzamide

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Chemical Property of 2-((2-[bis(pyridin-2-ylmethyl)amino]ethyl)amino)-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydroindazol-1-yl)benzamide

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Technology Process of 2-((2-[bis(pyridin-2-ylmethyl)amino]ethyl)amino)-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydroindazol-1-yl)benzamide

There total 3 articles about 2-((2-[bis(pyridin-2-ylmethyl)amino]ethyl)amino)-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydroindazol-1-yl)benzamide 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: 82.0%

: 1392213-67-0
2-((2-[bis(pyridin-2-ylmethyl)amino]ethyl)amino)-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydroindazol-1-yl)benzonitrile

: 1392213-63-6
2-((2-[bis(pyridin-2-ylmethyl)amino]ethyl)amino)-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydroindazol-1-yl)benzamide

Guidance literature:: With dihydrogen peroxide; potassium hydroxide; In ethanol; dimethyl sulfoxide; at 50 ℃; for 4h;
DOI:10.1039/c2ob25852h

Reference yield:

: 57381-39-2
2-bromo-5-fluorobenzonitrile

: 1392213-63-6
2-((2-[bis(pyridin-2-ylmethyl)amino]ethyl)amino)-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydroindazol-1-yl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / N,N-dimethyl-formamide / 20 - 80 °C

2: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; palladium dichloride; sodium t-butanolate / toluene / 100 °C / Inert atmosphere

3: dihydrogen peroxide; potassium hydroxide / ethanol; dimethyl sulfoxide / 4 h / 50 °C

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; dihydrogen peroxide; potassium carbonate; potassium hydroxide; palladium dichloride; sodium t-butanolate; In ethanol; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene; 2: Buchwald-Hartwig coupling;
DOI:10.1039/c2ob25852h

Reference yield:

: 16315-16-5
3,6,6-trimethyl-1⁽²⁾,5,6,7-tetrahydro-4H-indazole-4-one

: 1392213-63-6
2-((2-[bis(pyridin-2-ylmethyl)amino]ethyl)amino)-5-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydroindazol-1-yl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / N,N-dimethyl-formamide / 20 - 80 °C

2: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; palladium dichloride; sodium t-butanolate / toluene / 100 °C / Inert atmosphere

3: dihydrogen peroxide; potassium hydroxide / ethanol; dimethyl sulfoxide / 4 h / 50 °C

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; dihydrogen peroxide; potassium carbonate; potassium hydroxide; palladium dichloride; sodium t-butanolate; In ethanol; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene; 2: Buchwald-Hartwig coupling;
DOI:10.1039/c2ob25852h