3-[(2R,4R)-4-{[5-(4-Methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]oxy}piperidin-2-yl]-propanoic acid

Base Information

Chemical Name:3-[(2R,4R)-4-{[5-(4-Methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]oxy}piperidin-2-yl]-propanoic acid
CAS No.:1073134-72-1
Molecular Formula:C₂₇H₂₇N₃O₅
Molecular Weight:473.528
Hs Code.:

Synonyms:3-[(2R,4R)-4-{[5-(4-Methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]oxy}piperidin-2-yl]-propanoic acid

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Chemical Property of 3-[(2R,4R)-4-{[5-(4-Methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]oxy}piperidin-2-yl]-propanoic acid

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Technology Process of 3-[(2R,4R)-4-{[5-(4-Methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]oxy}piperidin-2-yl]-propanoic acid

There total 9 articles about 3-[(2R,4R)-4-{[5-(4-Methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]oxy}piperidin-2-yl]-propanoic 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: 71.3%

: 1073136-66-9
3-[(2R,4R)-1-(tert-Butoxycarbonyl)-4-{[5-(4-methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]-oxy}piperidin-2-yl]propanoic acid

: 1073134-72-1
3-[(2R,4R)-4-{[5-(4-Methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]oxy}piperidin-2-yl]-propanoic acid

Guidance literature:: 3-[(2R,4R)-1-(tert-Butoxycarbonyl)-4-{[5-(4-methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]-oxy}piperidin-2-yl]propanoic acid; With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 0.5h;

With sodium hydroxide; In water; acetonitrile; pH=7;

Reference yield:

: (2E)-3-{(2S,4R)-4-hydroxy-1-[(1R)-1-phenylethyl]piperidin-2-yl}acrylic acid methyl ester

: 1073134-72-1
3-[(2R,4R)-4-{[5-(4-Methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]oxy}piperidin-2-yl]-propanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogen / palladium 10% on activated carbon / isopropyl alcohol / 20 °C

2.1: 1-tert-butyl-2,2,4,4,4-pentakis(dimethylamino)-2Λ⁵,4Λ⁵-catenadi(phosphazene) / N,N-dimethyl-formamide; tetrahydrofuran / 1 h / -10 - 0 °C

3.1: sodium hydroxide; water / methanol / 0 - 40 °C

3.2: pH 3

4.1: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C

4.2: pH 7

With water; hydrogen; 1-tert-butyl-2,2,4,4,4-pentakis(dimethylamino)-2Λ⁵,4Λ⁵-catenadi(phosphazene); trifluoroacetic acid; sodium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol;

Reference yield:

: 178035-48-8
(1R,5S)-2-((R)-1-phenylethyl)-6-oxa-2-azabicyclo[3.2.1]octan-7-one

: 1073134-72-1
3-[(2R,4R)-4-{[5-(4-Methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]oxy}piperidin-2-yl]-propanoic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: L-Selectride / tetrahydrofuran / 1 h / -78 °C

1.2: 1 h / -20 - 0 °C

1.3: pH 7 - 8

2.1: hydrogen / palladium 10% on activated carbon / isopropyl alcohol / 20 °C

3.1: 1-tert-butyl-2,2,4,4,4-pentakis(dimethylamino)-2Λ⁵,4Λ⁵-catenadi(phosphazene) / N,N-dimethyl-formamide; tetrahydrofuran / 1 h / -10 - 0 °C

4.1: sodium hydroxide; water / methanol / 0 - 40 °C

4.2: pH 3

5.1: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C

5.2: pH 7

With water; hydrogen; L-Selectride; 1-tert-butyl-2,2,4,4,4-pentakis(dimethylamino)-2Λ⁵,4Λ⁵-catenadi(phosphazene); trifluoroacetic acid; sodium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol;