methyl 2-(4-(4'-((5-(tert-butyl)-1,3,4-oxadiazol-2-yl)amino)-[1,1'-biphenyl]-4-yl)-7-oxabicyclo[2.2.1]heptan-1-yl)acetate

Base Information

• Chemical Name: methyl 2-(4-(4'-((5-(tert-butyl)-1,3,4-oxadiazol-2-yl)amino)-[1,1'-biphenyl]-4-yl)-7-oxabicyclo[2.2.1]heptan-1-yl)acetate
• CAS No.: 1477524-74-5
• Molecular Formula: C₂₇H₃₁N₃O₄
• Molecular Weight: 461.561
• Mol file: 1477524-74-5.mol

Synonyms:methyl 2-(4-(4'-((5-(tert-butyl)-1,3,4-oxadiazol-2-yl)amino)-[1,1'-biphenyl]-4-yl)-7-oxabicyclo[2.2.1]heptan-1-yl)acetate

Chemical Property of methyl 2-(4-(4'-((5-(tert-butyl)-1,3,4-oxadiazol-2-yl)amino)-[1,1'-biphenyl]-4-yl)-7-oxabicyclo[2.2.1]heptan-1-yl)acetate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of methyl 2-(4-(4'-((5-(tert-butyl)-1,3,4-oxadiazol-2-yl)amino)-[1,1'-biphenyl]-4-yl)-7-oxabicyclo[2.2.1]heptan-1-yl)acetate

There total 6 articles about methyl 2-(4-(4'-((5-(tert-butyl)-1,3,4-oxadiazol-2-yl)amino)-[1,1'-biphenyl]-4-yl)-7-oxabicyclo[2.2.1]heptan-1-yl)acetate 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:

(5-tert-butyl-[1,3,4]oxadiazol-2-yl)-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]amine (1477524-57-4) + methyl 2-(4-(4-bromophenyl)-7-oxabicyclo[2.2.1]heptan-1-yl)acetate (1477524-73-4) → methyl 2-(4-(4'-((5-(tert-butyl)-1,3,4-oxadiazol-2-yl)amino)-[1,1'-biphenyl]-4-yl)-7-oxabicyclo[2.2.1]heptan-1-yl)acetate (1477524-74-5)

Guidance literature:

With bis(di-tert-?butyl(4-?dimethylaminophenyl)?phosphine)?dichloropalladium(II); cesium fluoride; In 1,4-dioxane; water; at 90 ℃; for 2h; Inert atmosphere;

Reference yield:

1.4-dibromobenzene (106-37-6) → methyl 2-(4-(4'-((5-(tert-butyl)-1,3,4-oxadiazol-2-yl)amino)-[1,1'-biphenyl]-4-yl)-7-oxabicyclo[2.2.1]heptan-1-yl)acetate (1477524-74-5)

Guidance literature:

Multi-step reaction with 4 steps

1.1: magnesium; iodine / tetrahydrofuran / 0.5 h / 20 °C

1.2: 15.33 h / -78 - 20 °C

2.1: toluene-4-sulfonic acid / acetone; water / 1 h / 75 °C

3.1: sodium hydride / methanol; mineral oil / 0.5 h / 20 °C

3.2: 20 h / 20 °C

4.1: cesium fluoride; bis(di-tert-?butyl(4-?dimethylaminophenyl)?phosphine)?dichloropalladium(II) / water; 1,4-dioxane / 2 h / 90 °C / Inert atmosphere

With bis(di-tert-?butyl(4-?dimethylaminophenyl)?phosphine)?dichloropalladium(II); iodine; sodium hydride; toluene-4-sulfonic acid; magnesium; cesium fluoride; In tetrahydrofuran; 1,4-dioxane; methanol; water; acetone; mineral oil; 3.1: |Wittig Olefination / 3.2: |Wittig Olefination / 4.1: |Suzuki Coupling;

Reference yield:

4-(4-bromophenyl)-4-hydroxycyclohexan-1-one (1477524-71-2) → methyl 2-(4-(4'-((5-(tert-butyl)-1,3,4-oxadiazol-2-yl)amino)-[1,1'-biphenyl]-4-yl)-7-oxabicyclo[2.2.1]heptan-1-yl)acetate (1477524-74-5)

Guidance literature:

Multi-step reaction with 2 steps

1.1: sodium hydride / methanol; mineral oil / 0.5 h / 20 °C

1.2: 20 h / 20 °C

2.1: cesium fluoride; bis(di-tert-?butyl(4-?dimethylaminophenyl)?phosphine)?dichloropalladium(II) / water; 1,4-dioxane / 2 h / 90 °C / Inert atmosphere

With bis(di-tert-?butyl(4-?dimethylaminophenyl)?phosphine)?dichloropalladium(II); sodium hydride; cesium fluoride; In 1,4-dioxane; methanol; water; mineral oil; 1.1: |Wittig Olefination / 1.2: |Wittig Olefination / 2.1: |Suzuki Coupling;

upstream raw materials:

1.4-dibromobenzene

cyclohexanedione monoethylene ketal

4-Hydroxy-4-(p-bromophenyl)cyclohexanone ethylene ketal

4-(4-bromophenyl)-4-hydroxycyclohexan-1-one

Downstream raw materials:

2-(4-(4'-((5-(tert-butyl)-1,3,4-oxadiazol-2-yl)amino)-[1,1'-biphenyl]-4-yl)-7-oxabicyclo[2.2.1]heptan-1-yl)acetic acid