ethyl 4-[6-(5-(adamantan-1-yl)-2-hydroxy-4-(2-methoxyethoxymethoxy)phenyl)-2-phenylpyrimidin-4-yl]benzoate

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Chemical Name:ethyl 4-[6-(5-(adamantan-1-yl)-2-hydroxy-4-(2-methoxyethoxymethoxy)phenyl)-2-phenylpyrimidin-4-yl]benzoate
CAS No.:1448617-93-3
Molecular Formula:C₃₉H₄₂N₂O₆
Molecular Weight:634.772
Hs Code.:

Synonyms:ethyl 4-[6-(5-(adamantan-1-yl)-2-hydroxy-4-(2-methoxyethoxymethoxy)phenyl)-2-phenylpyrimidin-4-yl]benzoate

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Chemical Property of ethyl 4-[6-(5-(adamantan-1-yl)-2-hydroxy-4-(2-methoxyethoxymethoxy)phenyl)-2-phenylpyrimidin-4-yl]benzoate

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Technology Process of ethyl 4-[6-(5-(adamantan-1-yl)-2-hydroxy-4-(2-methoxyethoxymethoxy)phenyl)-2-phenylpyrimidin-4-yl]benzoate

There total 5 articles about ethyl 4-[6-(5-(adamantan-1-yl)-2-hydroxy-4-(2-methoxyethoxymethoxy)phenyl)-2-phenylpyrimidin-4-yl]benzoate 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: 46.0%

: 1448617-92-2
ethyl 4-[6-(5-(adamantan-1-yl)-2,4-bis(2-methoxyethoxymethoxy)phenyl)-2-phenylpyrimidin-4-yl]benzoate

: 1448617-93-3
ethyl 4-[6-(5-(adamantan-1-yl)-2-hydroxy-4-(2-methoxyethoxymethoxy)phenyl)-2-phenylpyrimidin-4-yl]benzoate

Guidance literature:: With boron trichloride; In hexane; dichloromethane; at -78 ℃; for 18h; Inert atmosphere;
DOI:10.1002/cmdc.201300100

Reference yield:

: 173190-78-8
5-(adamantan-1-yl)-2,4-bis(2-methoxyethoxymethoxy)benzaldehyde

: 1448617-93-3
ethyl 4-[6-(5-(adamantan-1-yl)-2-hydroxy-4-(2-methoxyethoxymethoxy)phenyl)-2-phenylpyrimidin-4-yl]benzoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: diisopropylamine; n-butyllithium / hexane; tetrahydrofuran / 1 h / -78 - 0 °C / Inert atmosphere

1.2: 19 h / -78 - 25 °C / Inert atmosphere

2.1: pyridine; chromium(VI) oxide / dichloromethane / 4 h / 0 - 25 °C / Inert atmosphere

3.1: sodium carbonate / acetonitrile / 2 h / 120 °C / Microwave irradiation; Inert atmosphere

4.1: boron trichloride / hexane; dichloromethane / 18 h / -78 °C / Inert atmosphere

With pyridine; chromium(VI) oxide; n-butyllithium; boron trichloride; sodium carbonate; diisopropylamine; In tetrahydrofuran; hexane; dichloromethane; acetonitrile;
DOI:10.1002/cmdc.201300100

Reference yield:

: 1448617-80-8
ethyl 4-[1-(5-(adamantan-1-yl)-2,4-bis[(2-methoxyethoxy)methoxy]phenyl)prop-2-yn-1-ol-3-yl]benzoate

: 1448617-93-3
ethyl 4-[6-(5-(adamantan-1-yl)-2-hydroxy-4-(2-methoxyethoxymethoxy)phenyl)-2-phenylpyrimidin-4-yl]benzoate

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine; chromium(VI) oxide / dichloromethane / 4 h / 0 - 25 °C / Inert atmosphere

2: sodium carbonate / acetonitrile / 2 h / 120 °C / Microwave irradiation; Inert atmosphere

3: boron trichloride / hexane; dichloromethane / 18 h / -78 °C / Inert atmosphere

With pyridine; chromium(VI) oxide; boron trichloride; sodium carbonate; In hexane; dichloromethane; acetonitrile;
DOI:10.1002/cmdc.201300100