Hydrochloric Acid → N-{2-Amino-1-[3-(trifluoromethyl)phenyl]ethyl}-2-{3-(4-chlorophenyl)-5-oxo-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-4,5-dihydro-1H-1,2,4-triazol-1-yl}acetamide hydrochloride

HRID 2402834

Reaktionsgleichung

Reaktionsgleichung von HRID 2402834
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:12]([CH2:13][C@H:14]([OH:19])[C:15]([F:18])([F:17])[F:16])[C:11](=[O:20])[N:10]([CH2:21][C:22]([NH:24][CH:25]([C:30]3[CH:35]=[CH:34][CH:33]=[C:32]([C:36]([F:39])([F:38])[F:37])[CH:31]=3)[CH2:26][N+:27]([O-])=O)=[O:23])[N:9]=2)=[CH:4][CH:3]=1.[In].Cl>C1COCC1>[ClH:1].[NH2:27][CH2:26][CH:25]([NH:24][C:22](=[O:23])[CH2:21][N:10]1[C:11](=[O:20])[N:12]([CH2:13][C@H:14]([OH:19])[C:15]([F:18])([F:16])[F:17])[C:8]([C:5]2[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=2)=[N:9]1)[C:30]1[CH:35]=[CH:34][CH:33]=[C:32]([C:36]([F:38])([F:37])[F:39])[CH:31]=1

Komponenten

5

Versuchsvorschrift

Of the compound from Example 1, 45 mg (77 μmol) and 40 mg (348 μmol) of indium powder were admixed in 0.5 ml of THF with 42 μl of conc. hydrochloric acid, and the mixture was stirred at RT for 2 h. Then the mixture was purified by preparative HPLC (Method 10). The product-containing fractions were admixed with 2 ml of 1N hydrochloric acid and concentrated on a rotary evaporator. Drying in an HV gave 21 mg (46% of theory) of the title compound as a diastereomer mixture.

Aufarbeitung

  1. customThen the mixture was purified by preparative HPLC (Method 10)
  2. concentrationconcentrated on a rotary evaporator
  3. customDrying in an HV

Quellen und Nachweise

ORD-Eintrag
ord-5179967580664d8a857c85baa363b240
Quelldatensatz
uspto-grants-2014_08
Patentnummer
US08796324B2

Verknüpfte Notizen

Wird geladen…