Technology Process of (1R,2R,4R)-2-azido-4-(benzyloxy)cyclopentyl methanesulfonate
There total 6 articles about (1R,2R,4R)-2-azido-4-(benzyloxy)cyclopentyl methanesulfonate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
triethylamine;
In
dichloromethane;
at 0 - 20 ℃;
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: 180 °C / 760.05 Torr / Inert atmosphere
2.1: borane-THF; rac-α-pinene / 20.67 h / 0 - 20 °C / Inert atmosphere
2.2: 5 °C
3.1: sodium hydride / tetrahydrofuran; mineral oil / 0 °C
3.2: 6.75 h / 0 - 20 °C
4.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0 - 20 °C
5.1: sodium azide; ammonium chloride / ethanol; water / Reflux
6.1: triethylamine / dichloromethane / 0 - 20 °C
With
sodium azide; borane-THF; rac-α-pinene; sodium hydride; ammonium chloride; triethylamine; 3-chloro-benzenecarboperoxoic acid;
In
tetrahydrofuran; ethanol; dichloromethane; water; mineral oil;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: sodium hydride / tetrahydrofuran; mineral oil / 0 °C
1.2: 6.75 h / 0 - 20 °C
2.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0 - 20 °C
3.1: sodium azide; ammonium chloride / ethanol; water / Reflux
4.1: triethylamine / dichloromethane / 0 - 20 °C
With
sodium azide; sodium hydride; ammonium chloride; triethylamine; 3-chloro-benzenecarboperoxoic acid;
In
tetrahydrofuran; ethanol; dichloromethane; water; mineral oil;