C-{2-[5-(4-fluoro-phenyl)-4-pyridin-4-yl-1H-imidazol-2-yl]-5-methyl-[1,3]dioxan-5-yl}-methylamine

Base Information

Chemical Name:C-{2-[5-(4-fluoro-phenyl)-4-pyridin-4-yl-1H-imidazol-2-yl]-5-methyl-[1,3]dioxan-5-yl}-methylamine
CAS No.:218148-61-9
Molecular Formula:C₂₀H₂₁FN₄O₂
Molecular Weight:368.411
Hs Code.:

<i>C</i>-{2-[5-(4-fluoro-phenyl)-4-pyridin-4-yl-1<i>H</i>-imidazol-2-yl]-5-methyl-[1,3]dioxan-5-yl}-methylamine

Synonyms:C-{2-[5-(4-fluoro-phenyl)-4-pyridin-4-yl-1H-imidazol-2-yl]-5-methyl-[1,3]dioxan-5-yl}-methylamine

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Chemical Property of C-{2-[5-(4-fluoro-phenyl)-4-pyridin-4-yl-1H-imidazol-2-yl]-5-methyl-[1,3]dioxan-5-yl}-methylamine

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Technology Process of C-{2-[5-(4-fluoro-phenyl)-4-pyridin-4-yl-1H-imidazol-2-yl]-5-methyl-[1,3]dioxan-5-yl}-methylamine

There total 5 articles about C-{2-[5-(4-fluoro-phenyl)-4-pyridin-4-yl-1H-imidazol-2-yl]-5-methyl-[1,3]dioxan-5-yl}-methylamine 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: 9.0%

: 343304-90-5
t-2,2,2-trifluoro-N-[5-methyl-2-{5-(4-fluoro-phenyl)-4-pyridin-4-yl-1H-imidazol-2-yl}-[1,3]dioxan-r-5-ylmethyl]-acetamide

: 218148-61-9
C-{2-[5-(4-fluoro-phenyl)-4-pyridin-4-yl-1H-imidazol-2-yl]-5-methyl-[1,3]dioxan-5-yl}-methylamine

Guidance literature:: With water; potassium carbonate; In methanol; for 8h; Heating;
DOI:10.1016/S0968-0896(00)00331-X

Reference yield:

: 5-(4-fluoro-phenyl)-4-(4-pyridyl)-imidazole

: 218148-61-9
C-{2-[5-(4-fluoro-phenyl)-4-pyridin-4-yl-1H-imidazol-2-yl]-5-methyl-[1,3]dioxan-5-yl}-methylamine

Guidance literature:: Multi-step reaction with 5 steps

1.1: NaH / dimethylformamide / 1.5 h / 20 °C

1.2: n-BuLi / tetrahydrofuran; hexane / -78 - 20 °C

1.3: 58 percent / p-TsOH / methanol / 5 h / Heating

2.1: 1.56 g / p-TsOH / tetrahydrofuran / 6 h / Heating

3.1: 0.980 g / HCOONH₄ / Pd/C / methanol / 3.5 h

4.1: 300 mg / Et₃N / CH₂Cl₂ / 4.5 h / 20 °C

5.1: 9 percent / K₂CO₃; H₂O / methanol / 8 h / Heating

With water; ammonium formate; sodium hydride; potassium carbonate; toluene-4-sulfonic acid; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; 1.1: alkylation / 1.2: formylation / 1.3: alkylation / 2.1: cyclocondensation / 3.1: reduction / 4.1: acylation / 5.1: deacylation;
DOI:10.1016/S0968-0896(00)00331-X

Reference yield:

: 343304-85-8
4-[2-dimethoxymethyl-5-(4-fluoro-phenyl)-1H-imidazol-4-yl]-pyridine

: 218148-61-9
C-{2-[5-(4-fluoro-phenyl)-4-pyridin-4-yl-1H-imidazol-2-yl]-5-methyl-[1,3]dioxan-5-yl}-methylamine

Guidance literature:: Multi-step reaction with 4 steps

1: 1.56 g / p-TsOH / tetrahydrofuran / 6 h / Heating

2: 0.980 g / HCOONH₄ / Pd/C / methanol / 3.5 h

3: 300 mg / Et₃N / CH₂Cl₂ / 4.5 h / 20 °C

4: 9 percent / K₂CO₃; H₂O / methanol / 8 h / Heating

With water; ammonium formate; potassium carbonate; toluene-4-sulfonic acid; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; 1: cyclocondensation / 2: reduction / 3: acylation / 4: deacylation;
DOI:10.1016/S0968-0896(00)00331-X