2-[3-(2-fluoro-3-hydroxy-phenyl)propylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester

Base Information

Chemical Name:2-[3-(2-fluoro-3-hydroxy-phenyl)propylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester
CAS No.:1400705-79-4
Molecular Formula:C₁₈H₂₂FN₃O₃
Molecular Weight:347.389
Hs Code.:

Synonyms:2-[3-(2-fluoro-3-hydroxy-phenyl)propylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester

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Chemical Property of 2-[3-(2-fluoro-3-hydroxy-phenyl)propylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester

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Technology Process of 2-[3-(2-fluoro-3-hydroxy-phenyl)propylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester

There total 7 articles about 2-[3-(2-fluoro-3-hydroxy-phenyl)propylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester 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: 81.0%

: 1400705-78-3
2-[3-(2-fluoro-3-methoxy-phenyl)propylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester

: 1400705-79-4
2-[3-(2-fluoro-3-hydroxy-phenyl)propylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester

Guidance literature:: 2-[3-(2-fluoro-3-methoxy-phenyl)propylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester; With boron tribromide; In dichloromethane; at 0 - 20 ℃; for 2h;

With water; In dichloromethane; Cooling with ice;

Reference yield:

: 141-97-9
ethyl acetoacetate

: 1400705-79-4
2-[3-(2-fluoro-3-hydroxy-phenyl)propylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: acetic acid / ethanol / 90 °C

2.1: nitric acid / 0.25 h / 0 °C

2.2: Cooling with ice

3.1: N-ethyl-N,N-diisopropylamine; trichlorophosphate / 2 h / 110 °C

4.1: ethanol / 1 h / 160 °C / microwave irradiation

4.2: 20 °C

5.1: potassium carbonate; silver(II) oxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / dichloromethane / 72 h / 20 °C

6.1: hydrogen / palladium 10% on activated carbon / ethanol / 40 °C / 30003 Torr / H-Cube

7.1: boron tribromide / dichloromethane / 2 h / 0 - 20 °C

7.2: Cooling with ice

With silver(II) oxide; hydrogen; nitric acid; boron tribromide; potassium carbonate; N-ethyl-N,N-diisopropylamine; trichlorophosphate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; palladium 10% on activated carbon; acetic acid; In ethanol; dichloromethane;

Reference yield:

: 168130-75-4
4,6-dimethyl-2-hydroxypyrimidine-5-carboxylic acid ethyl ester

: 1400705-79-4
2-[3-(2-fluoro-3-hydroxy-phenyl)propylamino]-4,6-dimethyl-pyrimidine-5-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-ethyl-N,N-diisopropylamine; trichlorophosphate / 2 h / 110 °C

2.1: ethanol / 1 h / 160 °C / microwave irradiation

2.2: 20 °C

3.1: potassium carbonate; silver(II) oxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / dichloromethane / 72 h / 20 °C

4.1: hydrogen / palladium 10% on activated carbon / ethanol / 40 °C / 30003 Torr / H-Cube

5.1: boron tribromide / dichloromethane / 2 h / 0 - 20 °C

5.2: Cooling with ice

With silver(II) oxide; hydrogen; boron tribromide; potassium carbonate; N-ethyl-N,N-diisopropylamine; trichlorophosphate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; palladium 10% on activated carbon; In ethanol; dichloromethane;