5-benzyloxy-6-hydroxy-2-[1-(4-trifluoromethylphenyl)cyclopentylmethyl]pyrimidine-4-carboxylic acid

Base Information

Chemical Name:5-benzyloxy-6-hydroxy-2-[1-(4-trifluoromethylphenyl)cyclopentylmethyl]pyrimidine-4-carboxylic acid
CAS No.:1616924-33-4
Molecular Formula:C₂₅H₂₃F₃N₂O₄
Molecular Weight:472.464
Hs Code.:

Synonyms:5-benzyloxy-6-hydroxy-2-[1-(4-trifluoromethylphenyl)cyclopentylmethyl]pyrimidine-4-carboxylic acid

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Chemical Property of 5-benzyloxy-6-hydroxy-2-[1-(4-trifluoromethylphenyl)cyclopentylmethyl]pyrimidine-4-carboxylic acid

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Technology Process of 5-benzyloxy-6-hydroxy-2-[1-(4-trifluoromethylphenyl)cyclopentylmethyl]pyrimidine-4-carboxylic acid

There total 9 articles about 5-benzyloxy-6-hydroxy-2-[1-(4-trifluoromethylphenyl)cyclopentylmethyl]pyrimidine-4-carboxylic 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: 93.13%

: 1616924-32-3
5-benzyloxy-6-hydroxy-2-[1-(4-trifluoromethylphenyl)cyclopentylmethyl]pyrimidine-4-carboxylic acid tert-butyl ester

: 1616924-33-4
5-benzyloxy-6-hydroxy-2-[1-(4-trifluoromethylphenyl)cyclopentylmethyl]pyrimidine-4-carboxylic acid

Guidance literature:: With lithium hydroxide monohydrate; In tetrahydrofuran; water; for 20h; Reflux;

Reference yield:

: 1616924-30-1
[1-(4-trifluoromethylphenyl)cyclopentyl]acetonitrile

: 1616924-33-4
5-benzyloxy-6-hydroxy-2-[1-(4-trifluoromethylphenyl)cyclopentylmethyl]pyrimidine-4-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: ammonium chloride; trimethylaluminum / toluene / 16 h / 0 - 80 °C

2: sodium methylate / methanol / 16 h / 0 - 20 °C

3: lithium hydroxide monohydrate / tetrahydrofuran; water / 20 h / Reflux

With lithium hydroxide monohydrate; trimethylaluminum; sodium methylate; ammonium chloride; In tetrahydrofuran; methanol; water; toluene;

Reference yield:

: 30379-55-6
benzyloxyacetic acid

: 1616924-33-4
5-benzyloxy-6-hydroxy-2-[1-(4-trifluoromethylphenyl)cyclopentylmethyl]pyrimidine-4-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: thionyl chloride / 3 h / 0 - 20 °C

2: n-butyllithium; diisopropylamine / hexane; tetrahydrofuran / 2 h / -78 - 20 °C

3: sodium methylate / methanol / 16 h / 0 - 20 °C

4: lithium hydroxide monohydrate / tetrahydrofuran; water / 20 h / Reflux

With n-butyllithium; thionyl chloride; lithium hydroxide monohydrate; sodium methylate; diisopropylamine; In tetrahydrofuran; methanol; hexane; water;