(2S)-2-[[2-(3,5-difluorophenyl)acetyl]amino]propanoic acid → 4-(N'-(3,5-Difluorophenylacetyl)-L-alaninyl)amino-4-phenyl-1,2,3,4-tetrahydroisoquinolin-3-one

HRID 411343Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 411343
[F:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]([NH:12][C@H:13]([C:15]([OH:17])=O)[CH3:14])=[O:11])[CH:5]=[C:6]([F:8])[CH:7]=1.[NH2:18][CH:19]1[C:28]2[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=2)[CH:22](C2C=NC=CC=2)[NH:21][C:20]1=[O:35]>>[F:8][C:6]1[CH:5]=[C:4]([CH2:9][C:10]([NH:12][C@H:13]([C:15]([NH:18][C:19]2([C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)[C:28]3[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=3)[CH2:22][NH:21][C:20]2=[O:35])=[O:17])[CH3:14])=[O:11])[CH:3]=[C:2]([F:1])[CH:7]=1

Komponenten

3

Versuchsvorschrift

Following General Procedure D above using N-(3,5-difluorophenylacetyl)-L-alanine (Example B) and 4-amino-6-phenyl-1,2,3,4-tetrahydroisoquinoline-3-one (General Procedure 5-D), the title compound was prepared. The product was purified by LC 2000 chromatography, eluting with ethyl acetate.

Aufarbeitung

  1. customThe product was purified by LC 2000 chromatography
  2. washeluting with ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-fc6d75b237034f57908c9732cf631003
Quelldatensatz
uspto-grants-2003_05
Patentnummer
US06559141B2

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