Technology Process of (S)-tert-butyl 3-(4-benzoyl-2-(2-hydroxyethyl)piperazin-1-yl)propanoate
There total 5 articles about (S)-tert-butyl 3-(4-benzoyl-2-(2-hydroxyethyl)piperazin-1-yl)propanoate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: triethylamine / 65 - 75 °C / Inert atmosphere; Large scale reaction
1.2: 4 h / 20 °C / Inert atmosphere; Large scale reaction
2.1: tetrahydrofuran / 48 h / 50 - 60 °C / Inert atmosphere; Large scale reaction
With
triethylamine;
In
tetrahydrofuran;
2.1: Michael addition;
DOI:10.1021/op2001854
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: lithium borohydride / tetrahydrofuran / 20 - 50 °C / Inert atmosphere; Large scale reaction
1.2: 4.25 h / 40 - 50 °C / Inert atmosphere; Large scale reaction
2.1: triethylamine / 65 - 75 °C / Inert atmosphere; Large scale reaction
2.2: 4 h / 20 °C / Inert atmosphere; Large scale reaction
3.1: tetrahydrofuran / 48 h / 50 - 60 °C / Inert atmosphere; Large scale reaction
With
lithium borohydride; triethylamine;
In
tetrahydrofuran;
3.1: Michael addition;
DOI:10.1021/op2001854
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: methanesulfonic acid / ethanol / 1 h / 60 - 70 °C / Inert atmosphere; Large scale reaction
1.2: 5 h / Inert atmosphere; Reflux; Large scale reaction
2.1: lithium borohydride / tetrahydrofuran / 20 - 50 °C / Inert atmosphere; Large scale reaction
2.2: 4.25 h / 40 - 50 °C / Inert atmosphere; Large scale reaction
3.1: triethylamine / 65 - 75 °C / Inert atmosphere; Large scale reaction
3.2: 4 h / 20 °C / Inert atmosphere; Large scale reaction
4.1: tetrahydrofuran / 48 h / 50 - 60 °C / Inert atmosphere; Large scale reaction
With
lithium borohydride; methanesulfonic acid; triethylamine;
In
tetrahydrofuran; ethanol;
4.1: Michael addition;
DOI:10.1021/op2001854