N-{1-[2-amino-6-(3-amino-1H-indazol-6-yl)-4-pyrimidinyl]-3-piperidinyl}benzamide

Base Information

Chemical Name:N-{1-[2-amino-6-(3-amino-1H-indazol-6-yl)-4-pyrimidinyl]-3-piperidinyl}benzamide
CAS No.:1227919-90-5
Molecular Formula:C₂₃H₂₄N₈O
Molecular Weight:428.497
Hs Code.:

Synonyms:N-{1-[2-amino-6-(3-amino-1H-indazol-6-yl)-4-pyrimidinyl]-3-piperidinyl}benzamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-{1-[2-amino-6-(3-amino-1H-indazol-6-yl)-4-pyrimidinyl]-3-piperidinyl}benzamide

Chemical Property:

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Technology Process of N-{1-[2-amino-6-(3-amino-1H-indazol-6-yl)-4-pyrimidinyl]-3-piperidinyl}benzamide

There total 6 articles about N-{1-[2-amino-6-(3-amino-1H-indazol-6-yl)-4-pyrimidinyl]-3-piperidinyl}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:

: 184637-48-7,172603-05-3
t-butyl piperidin-3-ylcarbamate

: 1227919-90-5
N-{1-[2-amino-6-(3-amino-1H-indazol-6-yl)-4-pyrimidinyl]-3-piperidinyl}benzamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: methanol; ethanol / 50 - 100 °C

2.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium hydrogencarbonate / 1,4-dioxane; water / 95 °C

3.1: hydrazine hydrate / ethanol / 80 - 100 °C

4.1: hydrogenchloride / water / 0 - 20 °C

5.1: sodium hydrogencarbonate / tetrahydrofuran; water / 0 - 20 °C

5.2: 72 h / 65 °C

6.1: ammonium hydroxide / water; acetonitrile

With hydrogenchloride; ammonium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium hydrogencarbonate; hydrazine hydrate; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; water; acetonitrile; 2.1: Suzuki coupling;
DOI:10.1021/jm101527u

Reference yield:

: N-{1-[2-amino-6-(3-amino-1H-indazol-6-yl)-4-pyrimidinyl]-3-piperidinyl}benzamide dihydrochloride

: 1227919-90-5
N-{1-[2-amino-6-(3-amino-1H-indazol-6-yl)-4-pyrimidinyl]-3-piperidinyl}benzamide

Guidance literature:: With ammonium hydroxide; In water; acetonitrile;

Reference yield:

: 1227911-09-2
1,1-dimethylethyl {1-[2-amino-6-(4-cyano-3-fluorophenyl)-4-pyrimidinyl]-3-piperidinyl}carbamate

: 1227919-90-5
N-{1-[2-amino-6-(3-amino-1H-indazol-6-yl)-4-pyrimidinyl]-3-piperidinyl}benzamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrazine hydrate / ethanol / 80 - 100 °C

2.1: hydrogenchloride / water / 0 - 20 °C

3.1: sodium hydrogencarbonate / tetrahydrofuran; water / 0 - 20 °C

3.2: 72 h / 65 °C

4.1: ammonium hydroxide / water; acetonitrile

With hydrogenchloride; ammonium hydroxide; sodium hydrogencarbonate; hydrazine hydrate; In tetrahydrofuran; ethanol; water; acetonitrile;
DOI:10.1021/jm101527u