N-(3-Nitrophenylacetyl)-L-alanine → Methyl N-[N-(3-nitrophenylacetyl)-L-alaninyl]-(S)-2-aminobutanoate

HRID 322761Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 322761
[N+:1]([C:4]1[CH:5]=[C:6]([CH2:10][C:11]([NH:13][C@H:14]([C:16]([OH:18])=O)[CH3:15])=[O:12])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].Cl.[NH2:20][C@@H:21]([CH2:26][CH3:27])[C:22]([O:24][CH3:25])=[O:23]>>[N+:1]([C:4]1[CH:5]=[C:6]([CH2:10][C:11]([NH:13][C@H:14]([C:16]([NH:20][C@@H:21]([CH2:26][CH3:27])[C:22]([O:24][CH3:25])=[O:23])=[O:18])[CH3:15])=[O:12])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2]

Komponenten

3

Edukt 2

HCID 53788870N-(3-Nitrophenylacetyl)-L-alanineHCID 71313169(S)-methyl 2-aminobutanoate hydrochloride

Produkt 1

HCID 22894965Methyl N-[N-(3-nitrophenylacetyl)-L-alaninyl]-(S)-2-aminobutanoate

Versuchsvorschrift

Following General Procedure C and using N-(3-nitrophenylacetyl)-L-alanine (from Example D11 above) and methyl (S)-2-aminobutanoate hydrochloride (prepared from (S)-(+)-2-aminobutyric acid (Aldrich) using General Procedure H), the title compound was prepared as a solid (mp=154-157° C.).

Quellen und Nachweise

ORD-Eintrag
ord-01302e7551d649d1bade33fd98e9c270
Quelldatensatz
uspto-grants-2001_04
Patentnummer
US06211235B1

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