Diisopropylethylamine → HCID 89964581, Verbindung

HRID 2275503Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2275503
[CH2:1]([C:4]1[CH:8]=[C:7]([C:9]([OH:11])=O)[O:6][N:5]=1)[CH2:2][CH3:3].CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[NH2:36][C@H:37]([CH2:46][C:47]1[CH:52]=[CH:51][C:50]([C:53]2[CH:58]=[C:57]([Cl:59])[CH:56]=[CH:55][C:54]=2[F:60])=[CH:49][CH:48]=1)[CH2:38][C@:39]([CH2:44][OH:45])([CH3:43])[C:40]([OH:42])=[O:41].CCN(C(C)C)C(C)C>CN(C=O)C>[Cl:59][C:57]1[CH:56]=[CH:55][C:54]([F:60])=[C:53]([C:50]2[CH:49]=[CH:48][C:47]([CH2:46][C@@H:37]([NH:36][C:9]([C:7]3[O:6][N:5]=[C:4]([CH2:1][CH2:2][CH3:3])[CH:8]=3)=[O:11])[CH2:38][C@:39]([CH2:44][OH:45])([CH3:43])[C:40]([OH:42])=[O:41])=[CH:52][CH:51]=2)[CH:58]=1

Komponenten

6

Versuchsvorschrift

3-Propylisoxazole-5-carboxylic acid (9 mg, 55 μmol) and HATU (20.8 mg, 55 μmol) were combined in DMF (0.2 mL) and allowed to stand at room temperature for 10 minutes. (2S,4R)-4-Amino-5-(5′-chloro-2′-fluorobiphenyl-4-yl)-2-hydroxymethyl-2-methylpentanoic acid (20 mg, 55 μmol) in DMF and DIPEA (28.6 μL, 164 μmol) were added, and the resulting mixture was stirred for 20 minutes at room temperature. The mixture was concentrated under reduced pressure and the residue was dissolved in AcOH purified by preparative HPLC to yield the title compound (0.5 mg). MS m/z [M+H]+ calc'd for C26H28ClFN2O5, 503.17. found 504.2.

Aufarbeitung

  1. concentrationThe mixture was concentrated under reduced pressure
  2. dissolutionthe residue was dissolved in AcOH
  3. custompurified by preparative HPLC

Quellen und Nachweise

ORD-Eintrag
ord-44d74a44873e451bb6c6d00e251e5074
Quelldatensatz
uspto-grants-2015_09
Patentnummer
US09126956B2

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