Hydrazine → tert-butyl N-((1S)-1-(hydrazinecarbonyl)ethyl)carbamate
Reaktionsgleichung
[NH2:1][NH2:2].[C:3]([O:7][C:8]([NH:10][C@@H:11]([CH3:16])[C:12](OC)=[O:13])=[O:9])([CH3:6])([CH3:5])[CH3:4]>>[NH:1]([C:12](=[O:13])[C@@H:11]([NH:10][C:8](=[O:9])[O:7][C:3]([CH3:6])([CH3:5])[CH3:4])[CH3:16])[NH2:2]Komponenten
3
Reaktionsbedingungen
- Temperatur
- 72 °C
Versuchsvorschrift
A solution of hydrazine (234 mg, 7.31 mmol, 1.5 equv. in 8 ml of THF) was added to (S)-methyl 2-(tert-butoxycarbonylamino)propanoate (1000 mg, 4.88 mmol, 1.0 equv.), it was stirred in a sealed tube and refluxed (72° C.) overnight (18 hours), the solvent was removed to yield the desired product (880 mg, white solid) in 84% yield.
Aufarbeitung
- customthe solvent was removed
Quellen und Nachweise
- ORD-Eintrag
- ord-fda35eb829924fd1a8414ffaa95e0797
- Quelldatensatz
- uspto-grants-2015_02
- Patentnummer
- US08957068B2
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