4-amino-6-({1-[5-chloro-3-(5-cyanopyridin-3-yl)-4-fluoro-2-methoxyphenyl]ethyl}-amino)pyrimidine-5-carbonitrile

Base Information

Chemical Name:4-amino-6-({1-[5-chloro-3-(5-cyanopyridin-3-yl)-4-fluoro-2-methoxyphenyl]ethyl}-amino)pyrimidine-5-carbonitrile
CAS No.:1402000-14-9
Molecular Formula:C₂₀H₁₅ClFN₇O
Molecular Weight:423.837
Hs Code.:

Synonyms:4-amino-6-({1-[5-chloro-3-(5-cyanopyridin-3-yl)-4-fluoro-2-methoxyphenyl]ethyl}-amino)pyrimidine-5-carbonitrile

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Chemical Property of 4-amino-6-({1-[5-chloro-3-(5-cyanopyridin-3-yl)-4-fluoro-2-methoxyphenyl]ethyl}-amino)pyrimidine-5-carbonitrile

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Technology Process of 4-amino-6-({1-[5-chloro-3-(5-cyanopyridin-3-yl)-4-fluoro-2-methoxyphenyl]ethyl}-amino)pyrimidine-5-carbonitrile

There total 6 articles about 4-amino-6-({1-[5-chloro-3-(5-cyanopyridin-3-yl)-4-fluoro-2-methoxyphenyl]ethyl}-amino)pyrimidine-5-carbonitrile 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: 37.0%

: 402718-29-0
3-cyanopyridine-5-boronic acid pinacol ester

: 1402000-28-5
4-amino-6-{[1-(3-bromo-5-chloro-4-fluoro-2-methoxyphenyl)ethyl]amino}pyrimidine-5-carbonitrile

: 1402000-14-9
4-amino-6-({1-[5-chloro-3-(5-cyanopyridin-3-yl)-4-fluoro-2-methoxyphenyl]ethyl}-amino)pyrimidine-5-carbonitrile

Guidance literature:: With sodium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; water; at 90 ℃; for 2h; Inert atmosphere; microwave vial;

Reference yield:

: 865451-01-0
1-(5-chloro-4-fluoro-2-hydroxyphenyl)ethan-1-one

: 1402000-14-9
4-amino-6-({1-[5-chloro-3-(5-cyanopyridin-3-yl)-4-fluoro-2-methoxyphenyl]ethyl}-amino)pyrimidine-5-carbonitrile

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-Bromosuccinimide; acetic acid / 18 h / 20 °C

2.1: potassium carbonate / N,N-dimethyl-formamide / 1 h / 60 °C

3.1: ammonium acetate / acetonitrile; methanol / 1 h / 65 °C

3.2: 65 °C

4.1: N-ethyl-N,N-diisopropylamine / methanol / 100 °C

5.1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 2 h / 90 °C / Inert atmosphere; microwave vial

With N-Bromosuccinimide; ammonium acetate; sodium carbonate; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; methanol; water; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1382997-15-0
1-(3-bromo-5-chloro-4-fluoro-2-hydroxyphenyl)ethan-1-one

: 1402000-14-9
4-amino-6-({1-[5-chloro-3-(5-cyanopyridin-3-yl)-4-fluoro-2-methoxyphenyl]ethyl}-amino)pyrimidine-5-carbonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 1 h / 60 °C

2.1: ammonium acetate / acetonitrile; methanol / 1 h / 65 °C

2.2: 65 °C

3.1: N-ethyl-N,N-diisopropylamine / methanol / 100 °C

4.1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 2 h / 90 °C / Inert atmosphere; microwave vial

With ammonium acetate; sodium carbonate; potassium carbonate; N-ethyl-N,N-diisopropylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; methanol; water; N,N-dimethyl-formamide; acetonitrile;