ethyl 1-tert-butyl-5-(2-phenoxypyrimidin-4-yl)-1H-pyrazole-3-carboxylate

Base Information

Chemical Name:ethyl 1-tert-butyl-5-(2-phenoxypyrimidin-4-yl)-1H-pyrazole-3-carboxylate
CAS No.:1403333-73-2
Molecular Formula:C₂₀H₂₂N₄O₃
Molecular Weight:366.42
Hs Code.:
Mol file:1403333-73-2.mol

Synonyms:ethyl 1-tert-butyl-5-(2-phenoxypyrimidin-4-yl)-1H-pyrazole-3-carboxylate

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Chemical Property of ethyl 1-tert-butyl-5-(2-phenoxypyrimidin-4-yl)-1H-pyrazole-3-carboxylate

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Technology Process of ethyl 1-tert-butyl-5-(2-phenoxypyrimidin-4-yl)-1H-pyrazole-3-carboxylate

There total 4 articles about ethyl 1-tert-butyl-5-(2-phenoxypyrimidin-4-yl)-1H-pyrazole-3-carboxylate 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: 77.0%

: 1403333-68-5
ethyl 1-tert-butyl-5-[2-(methylsulfonyl)pyrimidin-4-yl]-1H-pyrazole-3-carboxylate

: 108-95-2,27073-41-2
phenol

: 1403333-73-2
ethyl 1-tert-butyl-5-(2-phenoxypyrimidin-4-yl)-1H-pyrazole-3-carboxylate

Guidance literature:: With potassium carbonate; N,N-dimethyl-formamide; at 70 ℃; for 3h;

Reference yield:

: 496863-48-0
1-(2-methylsulfanyl-pyrimidin-4-yl)-ethanone

: 1403333-73-2
ethyl 1-tert-butyl-5-(2-phenoxypyrimidin-4-yl)-1H-pyrazole-3-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium t-butanolate / tetrahydrofuran / -7 °C / Inert atmosphere

1.2: 2.5 h / -11 - 20 °C

2.1: sodium acetate; acetic acid / ethanol / 2 h / 80 °C

3.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0.5 h / 20 °C

4.1: potassium carbonate; N,N-dimethyl-formamide / 3 h / 70 °C

With sodium acetate; potassium carbonate; acetic acid; N,N-dimethyl-formamide; 3-chloro-benzenecarboperoxoic acid; sodium t-butanolate; In tetrahydrofuran; ethanol; dichloromethane;

Reference yield:

: 1403333-53-8
ethyl 4-[2-(methylsulfanyl)pyrimidin-4-yl]-2,4-dioxobutanoate

: 1403333-73-2
ethyl 1-tert-butyl-5-(2-phenoxypyrimidin-4-yl)-1H-pyrazole-3-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: sodium acetate; acetic acid / ethanol / 2 h / 80 °C

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0.5 h / 20 °C

3: potassium carbonate; N,N-dimethyl-formamide / 3 h / 70 °C

With sodium acetate; potassium carbonate; acetic acid; N,N-dimethyl-formamide; 3-chloro-benzenecarboperoxoic acid; In ethanol; dichloromethane;