N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino) benzamide

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Chemical Name:N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino) benzamide
CAS No.:1108743-80-1
Molecular Formula:C₃₀H₃₂F₂N₆O₂
Molecular Weight:546.62
Hs Code.:

Synonyms:N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino) benzamide

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Chemical Property of N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino) benzamide

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Technology Process of N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino) benzamide

There total 17 articles about N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino) 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: 64.0%

: N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-2-(2,2,2-trifluoro-N-(tetrahydro-2H-pyran-4-yl)acetamido)-4-(4-(2,2,2-trifluoroacetyl)piperazin-1-yl)benzamide

: 1108743-80-1
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino) benzamide

Guidance literature:: With potassium carbonate; In methanol; at 20 ℃; for 2h;

Reference yield:

: 214210-21-6
3-cyano-4-fluorophenylboronic acid

: 1108743-80-1
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino) benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: potassium phosphate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / toluene / 1.5 - 8 h / 100 °C / Inert atmosphere

2: hydrazine hydrate / butan-1-ol / Reflux

3: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 4 h / -20 °C

With potassium phosphate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; hydrazine hydrate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; toluene; butan-1-ol; 1: |Suzuki-Miyaura Coupling;
DOI:10.1021/acs.jmedchem.6b00064

Reference yield:

: 141776-91-2
1-bromomethyl-3,5-difluoro-benzene

: 1108743-80-1
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(piperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino) benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: potassium phosphate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / toluene / 1.5 - 8 h / 100 °C / Inert atmosphere

2: hydrazine hydrate / butan-1-ol / Reflux

3: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 4 h / -20 °C

With potassium phosphate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; hydrazine hydrate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; toluene; butan-1-ol; 1: |Suzuki-Miyaura Coupling;
DOI:10.1021/acs.jmedchem.6b00064