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Methanol → HCID 70657042, Verbindung

HRID 1504175
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1504175
[OH-].[Na+].CO.C[O:6][C:7](=[O:42])[C:8]1[CH:13]=[CH:12][C:11]([CH2:14][N:15]([CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][O:29][C:30]2[CH:31]=[C:32]3[C:37](=[CH:38][CH:39]=2)[N:36]([CH3:40])[C:35](=[O:41])[CH:34]=[CH:33]3)[CH2:16][CH2:17][C:18]2[CH:19]=[N:20][CH:21]=[CH:22][CH:23]=2)=[CH:10][CH:9]=1.O>C(O)(=O)C>[CH3:40][N:36]1[C:37]2[C:32](=[CH:31][C:30]([O:29][CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][N:15]([CH2:14][C:11]3[CH:12]=[CH:13][C:8]([C:7]([OH:42])=[O:6])=[CH:9][CH:10]=3)[CH2:16][CH2:17][C:18]3[CH:19]=[N:20][CH:21]=[CH:22][CH:23]=3)=[CH:39][CH:38]=2)[CH:33]=[CH:34][C:35]1=[O:41]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 887MethanolHCID 962WaterHCID 14798Sodium HydroxideHCID 706568124-{[[5-(1-Methyl-2-oxo-1,2-dihydroquinolin-6-yloxy)pentyl]-(2-pyridin-3-ylethyl)amino]methyl}benzoic acid methyl ester

Produkt 1

HCID 70657042HCID 70657042, VerbindungAusbeute 77,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

A 1N-sodium hydroxide aqueous solution(0.72 ml) was added to a methanol solution (2 ml) of 4-{[[5-(1-methyl-2-oxo-1,2-dihydroquinolin-6-yloxy)pentyl]-(2-pyridin-3-ylethyl)amino]methyl}benzoic acid methyl ester(153 mg). The mixture was stirred at 50° C. for 3 hours. The reaction mixture was condensed under reduced pressure. Water was added to the residue, and acetic acid was added for neutralization. The mixture was extracted using dichloromethane. The organic layer was dried with anhydrous sodium sulfate, and condensed under reduced pressure. Diisopropyl ether was added to the residue. The generated insoluble matter was separated by filtration and dried to give the title compound(115 mg) as a white powder.

Aufarbeitung

  1. customcondensed under reduced pressure
  2. additionwas added for neutralization
  3. extractionThe mixture was extracted
  4. dry with materialThe organic layer was dried with anhydrous sodium sulfate, and condensed under reduced pressure
  5. additionDiisopropyl ether was added to the residue
  6. customThe generated insoluble matter was separated by filtration
  7. customdried

Quellen und Nachweise

ORD-Eintrag
ord-c9aeccb5d06e4ca881479b411426cfee
Quelldatensatz
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09212187B2

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