2-methylpropionaldehyde O-[5-fluoro-4-(2-fluorobenzylamino)pyrimidin-2-yl]oxime

Base Information

Chemical Name:2-methylpropionaldehyde O-[5-fluoro-4-(2-fluorobenzylamino)pyrimidin-2-yl]oxime
CAS No.:1312324-06-3
Molecular Formula:C₁₅H₁₆F₂N₄O
Molecular Weight:306.315
Hs Code.:

Synonyms:2-methylpropionaldehyde O-[5-fluoro-4-(2-fluorobenzylamino)pyrimidin-2-yl]oxime

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Chemical Property of 2-methylpropionaldehyde O-[5-fluoro-4-(2-fluorobenzylamino)pyrimidin-2-yl]oxime

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Technology Process of 2-methylpropionaldehyde O-[5-fluoro-4-(2-fluorobenzylamino)pyrimidin-2-yl]oxime

There total 3 articles about 2-methylpropionaldehyde O-[5-fluoro-4-(2-fluorobenzylamino)pyrimidin-2-yl]oxime 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: 56.0%

: 151-00-8
isobutyraldehyde oxime

: 1312324-62-1
2-fluorobenzyl-(5-fluoro-2-methanesulfonyl-pyrimidin-4-yl)amine

: 1312324-06-3
2-methylpropionaldehyde O-[5-fluoro-4-(2-fluorobenzylamino)pyrimidin-2-yl]oxime

Guidance literature:: isobutyraldehyde oxime; With potassium tert-butylate; In tetrahydrofuran; at 20 ℃; for 0.25h;

2-fluorobenzyl-(5-fluoro-2-methanesulfonyl-pyrimidin-4-yl)amine; In tetrahydrofuran; at 20 ℃; for 16h;

Reference yield:

: 89-99-6
2-fluorobenzylamine

: 1312324-06-3
2-methylpropionaldehyde O-[5-fluoro-4-(2-fluorobenzylamino)pyrimidin-2-yl]oxime

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / tetrahydrofuran / 5 h / Reflux

2.1: ethanol / 10 h / Reflux

3.1: Oxone / water; methanol / 14.33 h / -45 - 10 °C

4.1: potassium tert-butylate / tetrahydrofuran / 0.25 h / 20 °C

4.2: 16 h / 20 °C

With Oxone; potassium tert-butylate; triethylamine; In tetrahydrofuran; methanol; ethanol; water;

Reference yield:

: 1174385-80-8
(2-chloro-5-fluoropyrimidin-4-yl)-(2-fluorobenzyl)amine

: 1312324-06-3
2-methylpropionaldehyde O-[5-fluoro-4-(2-fluorobenzylamino)pyrimidin-2-yl]oxime

Guidance literature:: Multi-step reaction with 3 steps

1.1: ethanol / 10 h / Reflux

2.1: Oxone / water; methanol / 14.33 h / -45 - 10 °C

3.1: potassium tert-butylate / tetrahydrofuran / 0.25 h / 20 °C

3.2: 16 h / 20 °C

With Oxone; potassium tert-butylate; In tetrahydrofuran; methanol; ethanol; water;