Parahydroxyatorvastatin

Base Information

• Chemical Name: Parahydroxyatorvastatin
• CAS No.: 214217-88-6
• Molecular Formula: C33H35 F N2 O6
• Molecular Weight: 574.649
• UNII: 9Q2QX99L5W
• Nikkaji Number: J996.541F
• Wikidata: Q27088372
• Mol file: 214217-88-6.mol

Synonyms:4-hydroxy-atorvastatin;4-hydroxyatorvastatin

Chemical Property of Parahydroxyatorvastatin

Chemical Property:

• Melting Point: 183-185°C
• Boiling Point: 759.0±60.0 °C(Predicted)
• PKA: 4.29±0.10(Predicted)
• PSA: 242.04000
• Density: 1.27±0.1 g/cm3(Predicted)
• LogP: 12.03020
• Storage Temp.: -20°C Freezer, Under Inert Atmosphere
• Solubility.: Methanol (Slightly)
• XLogP3: 4.6
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 12
• Exact Mass: 574.24791500
• Heavy Atom Count: 42
• Complexity: 854

Purity/Quality:

98%Min ^*data from raw suppliers

4-Hydroxy atorvastatin disodium salt ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)C1=C(C(=C(N1CCC(CC(CC(=O)O)O)O)C2=CC=C(C=C2)F)C3=CC=CC=C3)C(=O)NC4=CC=C(C=C4)O
• Isomeric SMILES: CC(C)C1=C(C(=C(N1CC[C@H](C[C@H](CC(=O)O)O)O)C2=CC=C(C=C2)F)C3=CC=CC=C3)C(=O)NC4=CC=C(C=C4)O
• Uses: Atorvastatin metabolite

Technology Process of Parahydroxyatorvastatin

There total 10 articles about Parahydroxyatorvastatin 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:

atorvastatin (134523-00-5,110862-48-1) → p-Hydroxyatorvastatin (214217-88-6) + o-Hydroxyatorvastatin (214217-86-4)

Guidance literature:

With chimera No_.17A₁V₂ derived from CYP₁₀₂A₁ mutant; In aq. phosphate buffer; dimethyl sulfoxide; Reagent/catalyst; Catalytic behavior; Enzymatic reaction;

Reference yield:

(3R,5R)-7-[2-(4-Fluoro-phenyl)-4-(4-hydroxy-phenylcarbamoyl)-5-isopropyl-3-phenyl-pyrrol-1-yl]-3,5-dihydroxy-heptanoic acid tert-butyl ester → p-Hydroxyatorvastatin (214217-88-6)

Guidance literature:

With sodium hydroxide; In tetrahydrofuran; water; at 20 ℃;

DOI:10.1002/(SICI)1099-1344(20000315)43:3<261::AID-JLCR312>3.0.CO;2-T

Reference yield:

p-benzyloxyaniline (6373-46-2) → p-Hydroxyatorvastatin (214217-88-6)

Guidance literature:

Multi-step reaction with 7 steps

1: 82 percent / toluene / Heating

2: β-alanine; glacial acetic acid / hexane / Heating

3: 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromide; triethylamine / ethanol / Heating

4: pivalic acid / tetrahydrofuran; toluene; heptane / Heating

5: 85 percent / hydrogen; acetic acid / palladium on carbon / ethyl acetate / 34 h / 2585.74 Torr

6: HCl / tetrahydrofuran; H₂O / 20 °C

7: sodium hydroxide / H₂O; tetrahydrofuran / 20 °C

With hydrogenchloride; sodium hydroxide; hydrogen; 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; acetic acid; triethylamine; 3-amino propanoic acid; Trimethylacetic acid; palladium on activated charcoal; In tetrahydrofuran; ethanol; hexane; n-heptane; water; ethyl acetate; toluene; 1: Acylation / 2: Condensation / 3: Addition / 4: Cycloaddition / 5: Hydrogenolysis / 6: Hydrolysis / 7: Hydrolysis;

DOI:10.1002/(SICI)1099-1344(20000315)43:3<261::AID-JLCR312>3.0.CO;2-T

upstream raw materials:

p-benzyloxyaniline

N-(4-(benzyloxy)phenyl)-4-methyl-3-oxopentanamide

2-benzylidene-N-(4-(benzyloxy)phenyl)-4-methyl-3-oxopentanamide

N-(4-(benzyloxy)phenyl)-2-(2-(4-fluorophenyl)-2-oxo-1-phenylethyl)-4-methyl-3-oxopentanamide

Downstream raw materials:

p-Hydroxyatorvastatin lactone