3-(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)propanoic acid

Base Information

Chemical Name:3-(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)propanoic acid
CAS No.:1477524-03-0
Molecular Formula:C₂₇H₃₁N₃O₄
Molecular Weight:461.561
Hs Code.:

Synonyms:3-(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)propanoic acid

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Chemical Property of 3-(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)propanoic acid

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Technology Process of 3-(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)propanoic acid

There total 6 articles about 3-(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)propanoic 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: 86.0%

: 1477524-79-0
methyl 3-(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)propanoate

: 1477524-03-0
3-(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)propanoic acid

Guidance literature:: With methanol; sodium hydroxide; In tetrahydrofuran; at 20 ℃; for 2h;

Reference yield:

: 1477524-76-7
1-(4-bromophenyl)-4-(iodomethyl)-7-oxabicyclo[2.2.1]heptane

: 1477524-03-0
3-(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)propanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydride / mineral oil; N,N-dimethyl acetamide / 0.5 h / 20 °C / Cooling with ice

1.2: 0.75 h / 150 °C / Microwave irradiation

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

3.1: methanol; sodium hydroxide / tetrahydrofuran / 2 h / 20 °C

With methanol; bis(di-tert-?butyl(4-?dimethylaminophenyl)?phosphine)?dichloropalladium(II); sodium hydride; cesium fluoride; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl acetamide; water; mineral oil; 2.1: |Suzuki Coupling;

Reference yield:

: 29648-66-6
4-methylenecyclohexanone

: 1477524-03-0
3-(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)propanoic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: magnesium; iodine / tetrahydrofuran / 1.5 h / 20 °C

1.2: 3.83 h / -78 - 20 °C

2.1: iodine; sodium carbonate / acetonitrile / 4.33 h / 20 °C

3.1: sodium hydride / mineral oil; N,N-dimethyl acetamide / 0.5 h / 20 °C / Cooling with ice

3.2: 0.75 h / 150 °C / Microwave irradiation

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

5.1: methanol; sodium hydroxide / tetrahydrofuran / 2 h / 20 °C

With methanol; bis(di-tert-?butyl(4-?dimethylaminophenyl)?phosphine)?dichloropalladium(II); iodine; sodium hydride; sodium carbonate; magnesium; cesium fluoride; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl acetamide; water; acetonitrile; mineral oil; 4.1: |Suzuki Coupling;