(1-biphenyl-4-ylmethyl-4-pyridin-4-yl-1H-pyrrol-3-yl)-imidazol-1-yl-methanone

Base Information

Chemical Name:(1-biphenyl-4-ylmethyl-4-pyridin-4-yl-1H-pyrrol-3-yl)-imidazol-1-yl-methanone
CAS No.:259816-87-0
Molecular Formula:C₂₆H₂₀N₄O
Molecular Weight:404.471
Hs Code.:

(1-biphenyl-4-ylmethyl-4-pyridin-4-yl-1<i>H</i>-pyrrol-3-yl)-imidazol-1-yl-methanone

Synonyms:(1-biphenyl-4-ylmethyl-4-pyridin-4-yl-1H-pyrrol-3-yl)-imidazol-1-yl-methanone

Suppliers and Price of (1-biphenyl-4-ylmethyl-4-pyridin-4-yl-1H-pyrrol-3-yl)-imidazol-1-yl-methanone

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Chemical Property of (1-biphenyl-4-ylmethyl-4-pyridin-4-yl-1H-pyrrol-3-yl)-imidazol-1-yl-methanone

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Technology Process of (1-biphenyl-4-ylmethyl-4-pyridin-4-yl-1H-pyrrol-3-yl)-imidazol-1-yl-methanone

There total 4 articles about (1-biphenyl-4-ylmethyl-4-pyridin-4-yl-1H-pyrrol-3-yl)-imidazol-1-yl-methanone 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:

: 1667-11-4
biphenyl-4-methylchloride

: 259816-87-0
(1-biphenyl-4-ylmethyl-4-pyridin-4-yl-1H-pyrrol-3-yl)-imidazol-1-yl-methanone

Guidance literature:: Multi-step reaction with 3 steps

1: 67 percent / tetrabutylammonium hydrogen sulfate; NaOH / CH₂Cl₂; H₂O / 15 h / 20 °C

2: 460 mg / NaOH / H₂O; ethanol / 15 h / 20 °C

3: 510 mg / tetrahydrofuran / 15 h / 20 °C

With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; In tetrahydrofuran; ethanol; dichloromethane; water;

Reference yield:

: 123293-78-7
ethyl 3-(4-pyridinyl)-(2E)-propenoate

: 259816-87-0
(1-biphenyl-4-ylmethyl-4-pyridin-4-yl-1H-pyrrol-3-yl)-imidazol-1-yl-methanone

Guidance literature:: Multi-step reaction with 4 steps

1: 99 percent / NaH / dimethylsulfoxide; diethyl ether / 0.25 h / 20 °C

2: 67 percent / tetrabutylammonium hydrogen sulfate; NaOH / CH₂Cl₂; H₂O / 15 h / 20 °C

3: 460 mg / NaOH / H₂O; ethanol / 15 h / 20 °C

4: 510 mg / tetrahydrofuran / 15 h / 20 °C

With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; sodium hydride; In tetrahydrofuran; diethyl ether; ethanol; dichloromethane; water; dimethyl sulfoxide;

Reference yield:

: 197774-66-6
ethyl 4-(4-pyridinyl)pyrrole-3-carboxylate

: 259816-87-0
(1-biphenyl-4-ylmethyl-4-pyridin-4-yl-1H-pyrrol-3-yl)-imidazol-1-yl-methanone

Guidance literature:: Multi-step reaction with 3 steps

1: 67 percent / tetrabutylammonium hydrogen sulfate; NaOH / CH₂Cl₂; H₂O / 15 h / 20 °C

2: 460 mg / NaOH / H₂O; ethanol / 15 h / 20 °C

3: 510 mg / tetrahydrofuran / 15 h / 20 °C

With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; In tetrahydrofuran; ethanol; dichloromethane; water;