Methane → HCID 178456073, Verbindung

HRID 865671

Reaktionsgleichung

Reaktionsgleichung von HRID 865671
[C:1]([N:3]=[C:4](OC1C=CC=CC=1)[NH:5][C:6]1[CH:7]=[N:8][C:9]([N:12]([CH3:14])[CH3:13])=[CH:10][CH:11]=1)#[N:2].[C:22]1([C@H:28]([NH2:31])[CH2:29][CH3:30])[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1.CN1CCOCC1.C>C(O)(C)C>[C:1]([N:3]=[C:4]([NH:31][C@@H:28]([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[CH2:29][CH3:30])[NH:5][C:6]1[CH:7]=[N:8][C:9]([N:12]([CH3:13])[CH3:14])=[CH:10][CH:11]=1)#[N:2]

Komponenten

6

Versuchsvorschrift

A stirred solution of the product from Step 4 (2.00 g, 0.00711 mol), (R)-(+)-1-phenylpropylamine (1.06 g, 0.00784 mol), N-methylmorpholine (1.69 ml, 0.0154 mol) and isopropanol (13.3 ml) was refluxed, under nitrogen, until the reaction was shown to be complete by TLC (28 hours). It was then concentrated and the residue chromatographed on silica gel with 1 to 4% MeOH-CHCl3. A solution of the product thus obtained in MeOH-EtOAc was decolorized with Darco (activated charcoal) and crystallized from EtOAc-hexane to give 1.02 g, m.p. 109°-111° C. and 0.120 g, m.p. 107°-113° C. of the titled product.

Aufarbeitung

  1. customto be complete by TLC (28 hours)
  2. concentrationIt was then concentrated
  3. customthe residue chromatographed on silica gel with 1 to 4% MeOH-CHCl3
  4. customA solution of the product thus obtained in MeOH-EtOAc
  5. customcrystallized from EtOAc-hexane

Quellen und Nachweise

ORD-Eintrag
ord-305b6d1802174bafaad6803f6180f433
Quelldatensatz
uspto-grants-1996_10
Patentnummer
US05567722

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