4-ethyl-2-[3-(3-hydroxy-phenyl)propylamino]-6-methyl-pyrimidine-5-carboxylic acid

Base Information

Chemical Name:4-ethyl-2-[3-(3-hydroxy-phenyl)propylamino]-6-methyl-pyrimidine-5-carboxylic acid
CAS No.:1400705-47-6
Molecular Formula:C₁₇H₂₁N₃O₃
Molecular Weight:315.372
Hs Code.:

Synonyms:4-ethyl-2-[3-(3-hydroxy-phenyl)propylamino]-6-methyl-pyrimidine-5-carboxylic acid

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

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

There total 6 articles about 4-ethyl-2-[3-(3-hydroxy-phenyl)propylamino]-6-methyl-pyrimidine-5-carboxylic acid 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: 98.0%

: 1400705-46-5
4-ethyl-2-[3-(3-hydroxy-phenyl)propylamino]-6-methyl-pyrimidine-5-carboxylic acid ethyl ester

: 1400705-47-6
4-ethyl-2-[3-(3-hydroxy-phenyl)propylamino]-6-methyl-pyrimidine-5-carboxylic acid

Guidance literature:: 4-ethyl-2-[3-(3-hydroxy-phenyl)propylamino]-6-methyl-pyrimidine-5-carboxylic acid ethyl ester; With lithium hydroxide monohydrate; water; In 1,4-dioxane; at 90 ℃; for 6h;

With potassium hydrogensulfate; In 1,4-dioxane; water; at 20 ℃; pH=2 - 4;

Reference yield:

: 4949-44-4
ethyl propanoylacetate

: 1400705-47-6
4-ethyl-2-[3-(3-hydroxy-phenyl)propylamino]-6-methyl-pyrimidine-5-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: hydrogenchloride / ethanol / 24 h / 80 °C / sealed tube

2.1: nitric acid / 0.08 h / 0 °C

2.2: 0 °C / pH 5 - 6

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

4.1: potassium acetate / ethanol / 1 h / 120 °C / microwave irradiation

4.2: 20 °C

5.1: boron tribromide / dichloromethane / 2 h / 20 °C / Cooling with ice-water

5.2: Cooling with ice

6.1: water; lithium hydroxide monohydrate / 1,4-dioxane / 6 h / 90 °C

6.2: 20 °C / pH 2 - 4

With lithium hydroxide monohydrate; water; nitric acid; potassium acetate; boron tribromide; N-ethyl-N,N-diisopropylamine; trichlorophosphate; hydrogenchloride; In 1,4-dioxane; ethanol; dichloromethane;

Reference yield:

: 1400705-45-4
4-ethyl-2-[3-(3-methoxy-phenyl)propylamino]-6-methyl-pyrimidine-5-carboxylic acid ethyl ester

: 1400705-47-6
4-ethyl-2-[3-(3-hydroxy-phenyl)propylamino]-6-methyl-pyrimidine-5-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: boron tribromide / dichloromethane / 2 h / 20 °C / Cooling with ice-water

1.2: Cooling with ice

2.1: water; lithium hydroxide monohydrate / 1,4-dioxane / 6 h / 90 °C

2.2: 20 °C / pH 2 - 4

With lithium hydroxide monohydrate; water; boron tribromide; In 1,4-dioxane; dichloromethane;