6-benzyl-1-(4-(4-fluorophenyl)butoxymethyl)-3-hydroxy-5-isopropylpyrimidine-2,4(1H,3H)-dione

Base Information

Chemical Name:6-benzyl-1-(4-(4-fluorophenyl)butoxymethyl)-3-hydroxy-5-isopropylpyrimidine-2,4(1H,3H)-dione
CAS No.:1281859-81-1
Molecular Formula:C₂₅H₂₉FN₂O₄
Molecular Weight:440.515
Hs Code.:

Synonyms:6-benzyl-1-(4-(4-fluorophenyl)butoxymethyl)-3-hydroxy-5-isopropylpyrimidine-2,4(1H,3H)-dione

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Chemical Property of 6-benzyl-1-(4-(4-fluorophenyl)butoxymethyl)-3-hydroxy-5-isopropylpyrimidine-2,4(1H,3H)-dione

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Technology Process of 6-benzyl-1-(4-(4-fluorophenyl)butoxymethyl)-3-hydroxy-5-isopropylpyrimidine-2,4(1H,3H)-dione

There total 4 articles about 6-benzyl-1-(4-(4-fluorophenyl)butoxymethyl)-3-hydroxy-5-isopropylpyrimidine-2,4(1H,3H)-dione 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: 64.0%

: 1281859-78-6
6-benzyl-1-(4-(4-fluorophenyl)butoxymethyl)-5-isopropylpyrimidine-2,4(1H,3H)-dione

: 1281859-81-1
6-benzyl-1-(4-(4-fluorophenyl)butoxymethyl)-3-hydroxy-5-isopropylpyrimidine-2,4(1H,3H)-dione

Guidance literature:: 6-benzyl-1-(4-(4-fluorophenyl)butoxymethyl)-5-isopropylpyrimidine-2,4(1H,3H)-dione; With sodium hydride; In tetrahydrofuran; at 0 - 20 ℃; for 1h; Inert atmosphere;

With 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/jm1014378

Reference yield:

: 40283-05-4
4-(4-fluorophenyl)-1-butanol

: 1281859-81-1
6-benzyl-1-(4-(4-fluorophenyl)butoxymethyl)-3-hydroxy-5-isopropylpyrimidine-2,4(1H,3H)-dione

Guidance literature:: Multi-step reaction with 3 steps

1.1: carbon tetrabromide; triphenylphosphine / tetrahydrofuran / 20 °C / Inert atmosphere

2.1: N,O-bis-(trimethylsilyl)-acetamide; tetra-(n-butyl)ammonium iodide / dichloromethane / 20 °C / Inert atmosphere

3.1: sodium hydride / tetrahydrofuran / 1 h / 0 - 20 °C / Inert atmosphere

3.2: 0 - 20 °C / Inert atmosphere

With N,O-bis-(trimethylsilyl)-acetamide; carbon tetrabromide; tetra-(n-butyl)ammonium iodide; sodium hydride; triphenylphosphine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm1014378

Reference yield:

: 589-06-0
4-(4-fluorophenyl)butanoic acid

: 1281859-81-1
6-benzyl-1-(4-(4-fluorophenyl)butoxymethyl)-3-hydroxy-5-isopropylpyrimidine-2,4(1H,3H)-dione

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 20 °C / Inert atmosphere

2.1: carbon tetrabromide; triphenylphosphine / tetrahydrofuran / 20 °C / Inert atmosphere

3.1: N,O-bis-(trimethylsilyl)-acetamide; tetra-(n-butyl)ammonium iodide / dichloromethane / 20 °C / Inert atmosphere

4.1: sodium hydride / tetrahydrofuran / 1 h / 0 - 20 °C / Inert atmosphere

4.2: 0 - 20 °C / Inert atmosphere

With lithium aluminium tetrahydride; N,O-bis-(trimethylsilyl)-acetamide; carbon tetrabromide; tetra-(n-butyl)ammonium iodide; sodium hydride; triphenylphosphine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm1014378