(E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridyl]-2-propen-1-ol

Base Information

Chemical Name:(E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridyl]-2-propen-1-ol
CAS No.:166253-89-0
Molecular Formula:C₁₉H₁₈N₂O₃
Molecular Weight:322.364
Hs Code.:

Synonyms:(E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridyl]-2-propen-1-ol

Suppliers and Price of (E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridyl]-2-propen-1-ol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridyl]-2-propen-1-ol

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Technology Process of (E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridyl]-2-propen-1-ol

There total 7 articles about (E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridyl]-2-propen-1-ol 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: 76.0%

: 166253-88-9
methyl (E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridyl]acrylate

: 166253-89-0
(E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridyl]-2-propen-1-ol

Guidance literature:: With diisobutylaluminium hydride; In hexane; dichloromethane; for 2h;
DOI:10.1248/cpb.50.100

Reference yield: 57.0%

: 166253-89-0
(E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridyl]-2-propen-1-ol

Guidance literature:

Reference yield:

: 4548-45-2
2-chloro-5-nitropyridine

: 166253-89-0
(E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridyl]-2-propen-1-ol

Guidance literature:: Multi-step reaction with 5 steps

1.1: 84 percent / NaH / dimethylformamide / 3 h

2.1: 81 percent / H₂ / 5 percent Pd/C / tetrahydrofuran; ethanol / 760 Torr

3.1: aq. NaNO₂; HBr / acetone / 0.5 h / 5 °C

3.2: 37 percent / Cu₂O / acetone

4.1: 83 percent / DBU / toluene / 2 h / 90 - 100 °C

5.1: 76 percent / DIBAL-H / hexane; CH₂Cl₂ / 2 h

With hydrogen bromide; hydrogen; sodium hydride; diisobutylaluminium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; sodium nitrite; palladium on activated charcoal; In tetrahydrofuran; ethanol; hexane; dichloromethane; N,N-dimethyl-formamide; acetone; toluene; 3.2: Meerwein arylation;
DOI:10.1248/cpb.50.100