Technology Process of (R)-4-[3,4-dimethyl-2,5-dioxo-4-(4-hydroxyphenyl)imidazolidin-1-yl]-2-methoxybenzonitrile
There total 9 articles about (R)-4-[3,4-dimethyl-2,5-dioxo-4-(4-hydroxyphenyl)imidazolidin-1-yl]-2-methoxybenzonitrile which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
(R)-4-[3,4-dimethyl-2,5-dioxo-4-(4-methoxyphenyl)imidazolidin-1-yl]-2-methoxybenzonitrile;
With
boron dimethyl-trifluoro sulphide;
In
dichloromethane;
at 20 ℃;
for 12h;
With
water; sodium hydrogencarbonate;
In
dichloromethane;
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: triethylamine / tetrahydrofuran / 2 h / Inert atmosphere; Reflux
2.1: sodium hydride / N,N-dimethyl acetamide; mineral oil / 0 °C / Inert atmosphere
2.2: 2 h / 20 °C / Inert atmosphere
3.1: boron dimethyl-trifluoro sulphide / dichloromethane / 12 h / 20 °C / Inert atmosphere
With
boron dimethyl-trifluoro sulphide; sodium hydride; triethylamine;
In
tetrahydrofuran; dichloromethane; N,N-dimethyl acetamide; mineral oil;
DOI:10.1021/jm300249m
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: (R)-1-phenyl-ethyl-amine / ethanol / 20 - 40 °C / Inert atmosphere
1.2: 0.75 h / 20 °C / pH 1 / Inert atmosphere
2.1: hydrogenchloride / 3 h / Inert atmosphere; Reflux
3.1: hydrogenchloride / 0 °C / Inert atmosphere; Reflux
3.2: Inert atmosphere
4.1: triethylamine / tetrahydrofuran / 2 h / Inert atmosphere; Reflux
5.1: sodium hydride / N,N-dimethyl acetamide; mineral oil / 0 °C / Inert atmosphere
5.2: 2 h / 20 °C / Inert atmosphere
6.1: boron dimethyl-trifluoro sulphide / dichloromethane / 12 h / 20 °C / Inert atmosphere
With
hydrogenchloride; boron dimethyl-trifluoro sulphide; (R)-1-phenyl-ethyl-amine; sodium hydride; triethylamine;
In
tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl acetamide; mineral oil;
DOI:10.1021/jm300249m