tert-butyl 5-(benzyloxy)-6-hydroxy-2-(2-methyl-2-phenylpropyl)pyrimidine-4-carboxylate

Base Information

• Chemical Name: tert-butyl 5-(benzyloxy)-6-hydroxy-2-(2-methyl-2-phenylpropyl)pyrimidine-4-carboxylate
• CAS No.: 1616923-06-8
• Molecular Formula: C₂₆H₃₀N₂O₄
• Molecular Weight: 434.535
• Mol file: 1616923-06-8.mol

Synonyms:tert-butyl 5-(benzyloxy)-6-hydroxy-2-(2-methyl-2-phenylpropyl)pyrimidine-4-carboxylate

Chemical Property of tert-butyl 5-(benzyloxy)-6-hydroxy-2-(2-methyl-2-phenylpropyl)pyrimidine-4-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of tert-butyl 5-(benzyloxy)-6-hydroxy-2-(2-methyl-2-phenylpropyl)pyrimidine-4-carboxylate

There total 7 articles about tert-butyl 5-(benzyloxy)-6-hydroxy-2-(2-methyl-2-phenylpropyl)pyrimidine-4-carboxylate 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: 21.0%

3-methyl-3-phenylbutanimidamide hydrochloride (1616923-05-7) + (E)-2-benzyloxy-3-hydroxybut-2-enedioic acid 4-tert-butyl ester 1-methyl ester → tert-butyl 5-(benzyloxy)-6-hydroxy-2-(2-methyl-2-phenylpropyl)pyrimidine-4-carboxylate (1616923-06-8)

Guidance literature:

With sodium methylate; In methanol; at 0 - 20 ℃;

Reference yield:

benzyloxyacetic acid (30379-55-6) → tert-butyl 5-(benzyloxy)-6-hydroxy-2-(2-methyl-2-phenylpropyl)pyrimidine-4-carboxylate (1616923-06-8)

Guidance literature:

Multi-step reaction with 3 steps

1: thionyl chloride / 3 h / 0 - 20 °C

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

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

With n-butyllithium; thionyl chloride; sodium methylate; diisopropylamine; In tetrahydrofuran; methanol; hexane;

Reference yield:

methyl 2-(benzyloxy)acetate (31600-43-8) → tert-butyl 5-(benzyloxy)-6-hydroxy-2-(2-methyl-2-phenylpropyl)pyrimidine-4-carboxylate (1616923-06-8)

Guidance literature:

Multi-step reaction with 2 steps

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

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

With n-butyllithium; sodium methylate; diisopropylamine; In tetrahydrofuran; methanol; hexane;

upstream raw materials:

benzyloxyacetic acid

methyl 2-(benzyloxy)acetate

3-methyl-3-phenylbutanimidamide hydrochloride

methyl 2-methyl-2-phenylpropionate

Downstream raw materials:

9-hydroxy-2-isopropyl-6-(2-methyl-2-phenylpropyl)-3,4-dihydro-2H-pyrazino[1,2-c]pyrimidine-1,8-dione

5-(benzyloxy)-6-hydroxy-2-(2-methyl-2-phenylpropyl)pyrimidine-4-carboxylic acid

5-(benzyloxy)-N-(2-(tert-butyldimethylsilyloxy)ethyl)-6-hydroxy-N-isopropyl-2-(2-methyl-2-phenylpropyl)pyrimidine-4-carboxamide

5-(benzyloxy)-6-hydroxy-N-(2-hydroxyethyl)-N-isopropyl-2-(2-methyl-2-phenylpropyl)pyrimidine-4-carboxamide