4-[(3R)-3-{[6-(2-Fluorophenyl)-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]oxy}piperidin-1-yl]butyric acid methyl ester

Base Information

Chemical Name:4-[(3R)-3-{[6-(2-Fluorophenyl)-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]oxy}piperidin-1-yl]butyric acid methyl ester
CAS No.:1073135-59-7
Molecular Formula:C₂₉H₃₀FN₃O₅
Molecular Weight:519.573
Hs Code.:

Synonyms:4-[(3R)-3-{[6-(2-Fluorophenyl)-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]oxy}piperidin-1-yl]butyric acid methyl ester

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Chemical Property of 4-[(3R)-3-{[6-(2-Fluorophenyl)-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]oxy}piperidin-1-yl]butyric acid methyl ester

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Technology Process of 4-[(3R)-3-{[6-(2-Fluorophenyl)-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]oxy}piperidin-1-yl]butyric acid methyl ester

There total 8 articles about 4-[(3R)-3-{[6-(2-Fluorophenyl)-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]oxy}piperidin-1-yl]butyric acid methyl 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: 22.0%

: 4897-84-1
Methyl 4-bromobutyrate

: 1073136-63-6
6-(2-fluorophenyl)-5-(4-methoxyphenyl)-4-[(3R)-piperidin-3-yloxy]furo[2,3-d]pyrimidine

: 1073135-59-7
4-[(3R)-3-{[6-(2-Fluorophenyl)-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]oxy}piperidin-1-yl]butyric acid methyl ester

Guidance literature:: With tetra-(n-butyl)ammonium iodide; potassium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide; at 70 - 80 ℃; for 26h;

Reference yield:

: 123-11-5
4-methoxy-benzaldehyde

: 1073135-59-7
4-[(3R)-3-{[6-(2-Fluorophenyl)-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]oxy}piperidin-1-yl]butyric acid methyl ester

Guidance literature:: Multi-step reaction with 8 steps

1.1: zinc(II) iodide / benzene / 1.58 h / 20 °C

2.1: diisopropylamine; n-butyllithium / hexane; 1,2-dimethoxyethane / 1 h / -60 °C

2.2: 4.33 h / -60 - 20 °C

2.3: 16 h / 20 °C

3.1: triethylamine / tetrahydrofuran / 20 °C / Cooling with ice

4.1: acetic anhydride / 0 °C

4.2: 24 h / 130 °C

5.1: trichlorophosphate / sulfolane / 1 h / 120 °C

5.2: 20 °C

6.1: sodium hydride / tetrahydrofuran; mineral oil / 0.17 h

6.2: 16 h / Reflux

7.1: formic acid / palladium / methanol / 21 h / 20 °C / Inert atmosphere

8.1: potassium carbonate; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide; tetrahydrofuran / 26 h / 70 - 80 °C

With n-butyllithium; formic acid; acetic anhydride; tetra-(n-butyl)ammonium iodide; sodium hydride; potassium carbonate; triethylamine; diisopropylamine; zinc(II) iodide; trichlorophosphate; palladium; In tetrahydrofuran; sulfolane; methanol; 1,2-dimethoxyethane; hexane; N,N-dimethyl-formamide; mineral oil; benzene;

Reference yield:

: 84126-12-5
2-(2-fluorophenyl)-2-hydroxy-1-(4-methoxyphenyl)ethanone

: 1073135-59-7
4-[(3R)-3-{[6-(2-Fluorophenyl)-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]oxy}piperidin-1-yl]butyric acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine / tetrahydrofuran / 20 °C / Cooling with ice

2.1: acetic anhydride / 0 °C

2.2: 24 h / 130 °C

3.1: trichlorophosphate / sulfolane / 1 h / 120 °C

3.2: 20 °C

4.1: sodium hydride / tetrahydrofuran; mineral oil / 0.17 h

4.2: 16 h / Reflux

5.1: formic acid / palladium / methanol / 21 h / 20 °C / Inert atmosphere

6.1: potassium carbonate; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide; tetrahydrofuran / 26 h / 70 - 80 °C

With formic acid; acetic anhydride; tetra-(n-butyl)ammonium iodide; sodium hydride; potassium carbonate; triethylamine; trichlorophosphate; palladium; In tetrahydrofuran; sulfolane; methanol; N,N-dimethyl-formamide; mineral oil;