{[(2-{[1-(4-tert-butylphenyl)piperidin-4-yl]methyl}-5-hydroxy-6-methylpyrimidin-4-yl)carbonyl]amino}acetic acid

Base Information

Chemical Name:{[(2-{[1-(4-tert-butylphenyl)piperidin-4-yl]methyl}-5-hydroxy-6-methylpyrimidin-4-yl)carbonyl]amino}acetic acid
CAS No.:1192161-74-2
Molecular Formula:C₂₄H₃₂N₄O₄
Molecular Weight:440.542
Hs Code.:

Synonyms:{[(2-{[1-(4-tert-butylphenyl)piperidin-4-yl]methyl}-5-hydroxy-6-methylpyrimidin-4-yl)carbonyl]amino}acetic acid

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Chemical Property of {[(2-{[1-(4-tert-butylphenyl)piperidin-4-yl]methyl}-5-hydroxy-6-methylpyrimidin-4-yl)carbonyl]amino}acetic acid

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Technology Process of {[(2-{[1-(4-tert-butylphenyl)piperidin-4-yl]methyl}-5-hydroxy-6-methylpyrimidin-4-yl)carbonyl]amino}acetic acid

There total 8 articles about {[(2-{[1-(4-tert-butylphenyl)piperidin-4-yl]methyl}-5-hydroxy-6-methylpyrimidin-4-yl)carbonyl]amino}acetic 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: 68.0%

: 1192164-08-1
ethyl {[(2-{[1-(4-tert-butylphenyl)piperidin-4-yl]methyl}-5-hydroxy-6-methylpyrimidin-4-yl)carbonyl]amino}acetate

: 1192161-74-2
{[(2-{[1-(4-tert-butylphenyl)piperidin-4-yl]methyl}-5-hydroxy-6-methylpyrimidin-4-yl)carbonyl]amino}acetic acid

Guidance literature:: ethyl {[(2-{[1-(4-tert-butylphenyl)piperidin-4-yl]methyl}-5-hydroxy-6-methylpyrimidin-4-yl)carbonyl]amino}acetate; With water; sodium hydroxide; In tetrahydrofuran; methanol; at 20 ℃; for 1h;

With hydrogenchloride; In water;

Reference yield:

: 1192163-99-7
tert-butyl 5-(benzyloxy)-2-{[1-(tert-butoxycarbonyl)piperidin-4-yl]methyl}-6-hydroxypyrimidine-4-carboxylate

: 1192161-74-2
{[(2-{[1-(4-tert-butylphenyl)piperidin-4-yl]methyl}-5-hydroxy-6-methylpyrimidin-4-yl)carbonyl]amino}acetic acid

Guidance literature:: Multi-step reaction with 8 steps

1.1: triethylamine / dichloromethane / 0.5 h / -78 °C

2.1: potassium carbonate; silver(l) oxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / tetrahydrofuran / 3 h / Reflux; Inert atmosphere

3.1: hydrogenchloride / ethyl acetate / 3 h / 20 °C

4.1: dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; sodium t-butanolate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / toluene / 8 h / Inert atmosphere; Reflux

5.1: water; sodium hydroxide / tetrahydrofuran; methanol / 1 h / 60 °C

5.2: 20 °C

6.1: 4-methyl-morpholine / tetrahydrofuran; ethanol / 0.08 h / 20 °C

6.2: 12 h / 20 °C

7.1: hydrogen / 5%-palladium/activated carbon / ethyl acetate / 2.5 h / 20 °C

8.1: water; sodium hydroxide / tetrahydrofuran; methanol / 1 h / 20 °C

With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; 4-methyl-morpholine; hydrogenchloride; water; hydrogen; potassium carbonate; triethylamine; sodium hydroxide; silver(l) oxide; sodium t-butanolate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; 5%-palladium/activated carbon; In tetrahydrofuran; methanol; ethanol; dichloromethane; ethyl acetate; toluene;

Reference yield:

: 1192164-01-4
tert-butyl 5-(benzyloxy)-2-{[1-(tert-butoxycarbonyl)piperidin-4-yl]methyl}-6-{[(trifluoromethyl)sulfonyl]oxy}pyrimidine-4-carboxylate

: 1192161-74-2
{[(2-{[1-(4-tert-butylphenyl)piperidin-4-yl]methyl}-5-hydroxy-6-methylpyrimidin-4-yl)carbonyl]amino}acetic acid

Guidance literature:: Multi-step reaction with 7 steps

1.1: potassium carbonate; silver(l) oxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / tetrahydrofuran / 3 h / Reflux; Inert atmosphere

2.1: hydrogenchloride / ethyl acetate / 3 h / 20 °C

3.1: dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; sodium t-butanolate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / toluene / 8 h / Inert atmosphere; Reflux

4.1: water; sodium hydroxide / tetrahydrofuran; methanol / 1 h / 60 °C

4.2: 20 °C

5.1: 4-methyl-morpholine / tetrahydrofuran; ethanol / 0.08 h / 20 °C

5.2: 12 h / 20 °C

6.1: hydrogen / 5%-palladium/activated carbon / ethyl acetate / 2.5 h / 20 °C

7.1: water; sodium hydroxide / tetrahydrofuran; methanol / 1 h / 20 °C

With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; 4-methyl-morpholine; hydrogenchloride; water; hydrogen; potassium carbonate; sodium hydroxide; silver(l) oxide; sodium t-butanolate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; 5%-palladium/activated carbon; In tetrahydrofuran; methanol; ethanol; ethyl acetate; toluene;