(E)-1-(4-(1-(4-fluorophenyl)-3-(2-(2,6,6-trimethylcyclohex-2-enyl)vinyl)-4,5-dihydro-1H-pyrazol-5-yl)phenyl)-1H-1,2,4-triazole

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Chemical Name:(E)-1-(4-(1-(4-fluorophenyl)-3-(2-(2,6,6-trimethylcyclohex-2-enyl)vinyl)-4,5-dihydro-1H-pyrazol-5-yl)phenyl)-1H-1,2,4-triazole
CAS No.:1432043-42-9
Molecular Formula:C₂₈H₃₀FN₅
Molecular Weight:455.578
Hs Code.:

Synonyms:(E)-1-(4-(1-(4-fluorophenyl)-3-(2-(2,6,6-trimethylcyclohex-2-enyl)vinyl)-4,5-dihydro-1H-pyrazol-5-yl)phenyl)-1H-1,2,4-triazole

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Chemical Property of (E)-1-(4-(1-(4-fluorophenyl)-3-(2-(2,6,6-trimethylcyclohex-2-enyl)vinyl)-4,5-dihydro-1H-pyrazol-5-yl)phenyl)-1H-1,2,4-triazole

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Technology Process of (E)-1-(4-(1-(4-fluorophenyl)-3-(2-(2,6,6-trimethylcyclohex-2-enyl)vinyl)-4,5-dihydro-1H-pyrazol-5-yl)phenyl)-1H-1,2,4-triazole

There total 2 articles about (E)-1-(4-(1-(4-fluorophenyl)-3-(2-(2,6,6-trimethylcyclohex-2-enyl)vinyl)-4,5-dihydro-1H-pyrazol-5-yl)phenyl)-1H-1,2,4-triazole 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: 46.0%

: 1432043-44-1
(1E,4E)-1-(4-(1H-1,2,4-triazol-1-yl)phenyl)-5-(2,6,6-trimethylcyclohex-2-enyl)penta-1,4-dien-3-one

: 823-85-8
4-fluorophenyhydrazine hydrochloride

: 1432043-42-9
(E)-1-(4-(1-(4-fluorophenyl)-3-(2-(2,6,6-trimethylcyclohex-2-enyl)vinyl)-4,5-dihydro-1H-pyrazol-5-yl)phenyl)-1H-1,2,4-triazole

Guidance literature:: In ethanol; for 8h; Reflux;
DOI:10.1016/j.bmcl.2013.03.055

Reference yield:

: 27996-86-7
4-(1H-1,2,4-triazol-1-yl)benzaldehyde

: 1432043-42-9
(E)-1-(4-(1-(4-fluorophenyl)-3-(2-(2,6,6-trimethylcyclohex-2-enyl)vinyl)-4,5-dihydro-1H-pyrazol-5-yl)phenyl)-1H-1,2,4-triazole

Guidance literature:: Multi-step reaction with 2 steps

1: cetyltrimethylammonim bromide; sodium hydroxide / water / 24 h / 20 °C

2: ethanol / 8 h / Reflux

With cetyltrimethylammonim bromide; sodium hydroxide; In ethanol; water;
DOI:10.1016/j.bmcl.2013.03.055