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Dimethylformamide → HCID 87235259, Verbindung

HRID 2194500
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2194500
[CH3:1][N:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([C:12]([F:15])([F:14])[F:13])[N:10]=2)[CH:5]=[C:4]([C:16](O)=[O:17])[C:3]1=[O:19].C(Cl)(=O)C([Cl:23])=O.CN(C)C=O>ClCCl>[CH3:1][N:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([C:12]([F:15])([F:14])[F:13])[N:10]=2)[CH:5]=[C:4]([C:16]([Cl:23])=[O:17])[C:3]1=[O:19]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6228DimethylformamideHCID 65578Oxalyl chlorideHCID 67009484HCID 67009484, Verbindung

Produkt 1

HCID 87235259HCID 87235259, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

0.83 g (3.0 mmol) of 1-methyl-2-oxo-7-(trifluoromethyl)-1,2-dihydro-1,8-naphthyridine-3-carboxylic acid was dissolved in dichloromethane (50 mL), and 1.0 mL (12 mmol) of oxalyl chloride was added thereto. Two droplets of N,N-dimethylformamide were added to the above mixture, and the resulting mixture was stirred for 2 hours at 40° C. The reaction solution was concentrated under reduced pressure, and thus 1-methyl-2-oxo-7-(trifluoromethyl)-1,2-dihydro-1,8-naphthyridine-3-carboxylic acid chloride was obtained. The acid chloride thus obtained was dissolved in acetonitrile (30 mL), and this solution was added to an acetonitrile (50 mL) solution of 0.38 g (3.4 mmol) of 1,3-cyclohexanedione and 0.51 mL (3.7 mmol) of triethylamine under ice cooling. The resulting mixture was stirred for 2 hours at room temperature. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The organic phase was washed with water, an aqueous solution of sodium hydrogen carbonate, and water in this order, and was dried and concentrated. The residue was washed with diisopropyl ether, and thus 0.51 g (yield: 46%) of the title compound was obtained as brown crystals.

Aufarbeitung

  1. concentrationThe reaction solution was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-69a5520f7fa7446e810c779815ec1b8a
Quelldatensatz
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08334236B2

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