Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1106999Erstellt: 27. Oktober 2026

(S)-(-)-N-Benzyl-1-phenylethylamine → N-{2-oxo-2-{(phenylmethyl)(1(S)-phenylethyl}amino}ethyl}carbamate hydrochloride

https://huagongshe.com/reaction/1106999

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(S)-(-)-N-Benzyl-1-phenylethylamineHCID 1268085—
Edukttert-butyl N-{2-oxo-2-{(phenylmethyl){1(S)-phenylethyl}amino}ethyl}carbamateHCID 21968351—
Edukt2-(phenylmethyl)amino-N-phenylmethyl-N-{1(S)phenylethyl}acetamide hydrochlorideHCID 23390399—
ProduktN-{2-oxo-2-{(phenylmethyl)(1(S)-phenylethyl}amino}ethyl}carbamate hydrochlorideHCID 70150879—

Reaktionsschritte

2-(phenylmethyl)amino-N-phenylmethyl-N-{1(S)phenylethyl}acetamide hydrochloride: By following the procedure of Example 1(a) but replacing dibenzylamine with α(S)-methyl-N-(phenylmethyl)benzene methanamine, ((S)-N-benzyl-α-methylbenzylamine, Oxford Asymmetry Ltd., Abingdon Oxon, UK), tert-butyl N-{2-oxo-2-{(phenylmethyl){1(S)-phenylethyl}amino}ethyl}carbamate was made. The Boc group was removed following the procedure of Example 1(b) to give N-{2-oxo-2-{(phenylmethyl){1(S)-phenylethyl}amino}ethyl}carbamate hydrochloride, which was subjected to reductive amination with benzaldehyde according the procedure of R. F. Borch, Org. Synth., 1972, 52, 124, to give 2-(phenylmethyl)amino-N-phenylmethyl-N-{1(S)-phenylethyl}acetamide hydrochloride.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06057451
Quelldatensatzuspto-grants-2000_05
ORD IDord-d4ebbc2ebbaa4982b6a43b6dd6ebc83b
Quellennotizuspto-grants-2000_05