2-{2-[4-(4-chloro-3-trifluoromethyl-phenoxy)-phenyl]-ethylamino}-5-(6-methylpyridin-3-ylmethyl)-1H-pyrimidin-4-one

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Chemical Name:2-{2-[4-(4-chloro-3-trifluoromethyl-phenoxy)-phenyl]-ethylamino}-5-(6-methylpyridin-3-ylmethyl)-1H-pyrimidin-4-one
CAS No.:1380429-12-8
Molecular Formula:C₂₆H₂₂ClF₃N₄O₂
Molecular Weight:514.934
Hs Code.:

Synonyms:2-{2-[4-(4-chloro-3-trifluoromethyl-phenoxy)-phenyl]-ethylamino}-5-(6-methylpyridin-3-ylmethyl)-1H-pyrimidin-4-one

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Chemical Property of 2-{2-[4-(4-chloro-3-trifluoromethyl-phenoxy)-phenyl]-ethylamino}-5-(6-methylpyridin-3-ylmethyl)-1H-pyrimidin-4-one

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Technology Process of 2-{2-[4-(4-chloro-3-trifluoromethyl-phenoxy)-phenyl]-ethylamino}-5-(6-methylpyridin-3-ylmethyl)-1H-pyrimidin-4-one

There total 5 articles about 2-{2-[4-(4-chloro-3-trifluoromethyl-phenoxy)-phenyl]-ethylamino}-5-(6-methylpyridin-3-ylmethyl)-1H-pyrimidin-4-one 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: 46.54%

: 1380429-35-5
2-(4-(4-chloro-3-(trifluoromethyl)phenoxy)phenyl)ethanamine

: 71351-50-3
2-methylthio-5-(2-methylpyrid-5-ylmethyl)-1H-pyrimid-4-one

: 1380429-12-8
2-{2-[4-(4-chloro-3-trifluoromethyl-phenoxy)-phenyl]-ethylamino}-5-(6-methylpyridin-3-ylmethyl)-1H-pyrimidin-4-one

Guidance literature:: With ethanol; at 130 ℃; for 20h; Sealed vial;

Reference yield:

: 459-57-4
4-fluorobenzaldehyde

: 1380429-12-8
2-{2-[4-(4-chloro-3-trifluoromethyl-phenoxy)-phenyl]-ethylamino}-5-(6-methylpyridin-3-ylmethyl)-1H-pyrimidin-4-one

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / N,N-dimethyl-formamide / 0.33 h / 120 °C / Microwave irradiation

2: ammonium acetate; acetic acid / 3 h / 120 °C

3: sodium tetrahydroborate; (+/-)-2-pentanol; silica gel / chloroform / 3 h / 20 °C

4: methanol; sodium tetrahydroborate; nickel(II) chloride hexahydrate / 0 - 20 °C

5: ethanol / 20 h / 130 °C / Sealed vial

With methanol; sodium tetrahydroborate; nickel(II) chloride hexahydrate; ethanol; (+/-)-2-pentanol; ammonium acetate; silica gel; potassium carbonate; acetic acid; In chloroform; N,N-dimethyl-formamide;

Reference yield:

: 516481-95-1
4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}benzaldehyde

: 1380429-12-8
2-{2-[4-(4-chloro-3-trifluoromethyl-phenoxy)-phenyl]-ethylamino}-5-(6-methylpyridin-3-ylmethyl)-1H-pyrimidin-4-one

Guidance literature:: Multi-step reaction with 4 steps

1: ammonium acetate; acetic acid / 3 h / 120 °C

2: sodium tetrahydroborate; (+/-)-2-pentanol; silica gel / chloroform / 3 h / 20 °C

3: methanol; sodium tetrahydroborate; nickel(II) chloride hexahydrate / 0 - 20 °C

4: ethanol / 20 h / 130 °C / Sealed vial

With methanol; sodium tetrahydroborate; nickel(II) chloride hexahydrate; ethanol; (+/-)-2-pentanol; ammonium acetate; silica gel; acetic acid; In chloroform;