2-(3-(4-((1H-indazol-5-yl)amino)-6-((2-dimethylamino)ethoxy)pyrimidin-2-yl)phenoxy)-N-isopropylacetamide

Base Information

Chemical Name:2-(3-(4-((1H-indazol-5-yl)amino)-6-((2-dimethylamino)ethoxy)pyrimidin-2-yl)phenoxy)-N-isopropylacetamide
CAS No.:1595290-08-6
Molecular Formula:C₂₆H₃₁N₇O₃
Molecular Weight:489.577
Hs Code.:

Synonyms:2-(3-(4-((1H-indazol-5-yl)amino)-6-((2-dimethylamino)ethoxy)pyrimidin-2-yl)phenoxy)-N-isopropylacetamide

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Chemical Property of 2-(3-(4-((1H-indazol-5-yl)amino)-6-((2-dimethylamino)ethoxy)pyrimidin-2-yl)phenoxy)-N-isopropylacetamide

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Technology Process of 2-(3-(4-((1H-indazol-5-yl)amino)-6-((2-dimethylamino)ethoxy)pyrimidin-2-yl)phenoxy)-N-isopropylacetamide

There total 4 articles about 2-(3-(4-((1H-indazol-5-yl)amino)-6-((2-dimethylamino)ethoxy)pyrimidin-2-yl)phenoxy)-N-isopropylacetamide 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: 16.0%

: 1595290-07-5
2-(3-(4-chloro-6-((2-dimethylamino)ethoxy)pyrimidin-2-yl)phenoxy)-N-isopropylacetamide

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

: 1595290-08-6
2-(3-(4-((1H-indazol-5-yl)amino)-6-((2-dimethylamino)ethoxy)pyrimidin-2-yl)phenoxy)-N-isopropylacetamide

Guidance literature:: With triethylamine; In ethanol; at 80 ℃;

Reference yield:

: 75726-96-4
2-bromo-N-isopropylacetamide

: 1595290-08-6
2-(3-(4-((1H-indazol-5-yl)amino)-6-((2-dimethylamino)ethoxy)pyrimidin-2-yl)phenoxy)-N-isopropylacetamide

Guidance literature:: Multi-step reaction with 4 steps

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

2: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate / water; 1,2-dimethoxyethane / Inert atmosphere; Reflux

3: sodium hydroxide / toluene / 3 h / 110 °C

4: triethylamine / ethanol / 80 °C

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate; potassium carbonate; triethylamine; sodium hydroxide; In 1,2-dimethoxyethane; ethanol; water; N,N-dimethyl-formamide; toluene;

Reference yield:

: 1595291-50-1
2-(3-(4,6-dichloropyrimidin-2-yl)phenoxy)-N-isopropylacetamide

: 1595290-08-6
2-(3-(4-((1H-indazol-5-yl)amino)-6-((2-dimethylamino)ethoxy)pyrimidin-2-yl)phenoxy)-N-isopropylacetamide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / toluene / 3 h / 110 °C

2: triethylamine / ethanol / 80 °C

With triethylamine; sodium hydroxide; In ethanol; toluene;