3-Fluorobenzyl chloride → 7-[(3-Fluorophenyl)methoxy]-1,5-naphthyridine-3-carboxamide

HRID 513961Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 513961
[F:1][C:2]1[CH:3]=[C:4]([CH:22]=[CH:23][CH:24]=1)[CH2:5][O:6][C:7]1[CH:16]=[C:15]2[C:10]([CH:11]=[C:12]([C:17](OCC)=[O:18])[CH:13]=[N:14]2)=[N:9][CH:8]=1.OC1C=C2C(C=C(C(OCC)=O)C=N2)=[N:28]C=1.C([O-])([O-])=O.[Cs+].[Cs+].FC1C=C(C=CC=1)CCl>CN(C=O)C.O.CCOC(C)=O>[F:1][C:2]1[CH:3]=[C:4]([CH2:5][O:6][C:7]2[CH:16]=[C:15]3[C:10]([CH:11]=[C:12]([C:17]([NH2:28])=[O:18])[CH:13]=[N:14]3)=[N:9][CH:8]=2)[CH:22]=[CH:23][CH:24]=1

Komponenten

8

Edukt 4

HCID 99743-Fluorobenzyl chlorideHCID 10796Cesium carbonateHCID 90417603Ethyl 7-((3-fluorobenzyl)oxy)-1,5-naphthyridine-3-carboxylateHCID 136227102Ethyl 7-hydroxy-1,5-naphthyridine-3-carboxylate2×

Produkt 1

HCID 862964697-[(3-Fluorophenyl)methoxy]-1,5-naphthyridine-3-carboxamideAusbeute 69 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 962WaterLösungsmittelHCID 6228DimethylformamideLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

Ethyl 7-((3-fluorobenzyl)oxy)-1,5-naphthyridine-3-carboxylate. To a solution of ethyl 7-hydroxy-1,5-naphthyridine-3-carboxylate (Intermediate 4, 1.0 g, 4.59 mmol) in DMF (20 mL) was added Cs2CO3 (2.2 g, 6.75 mmol), followed by 3-fluorobenzyl chloride (0.6 mL, 5.02 mmol). The reaction was stirred at ambient temperature for 72 h. The crude reaction mixture was poured into EtOAc and water. The aqueous later was extracted with EtOAc and the combined organic fractions were washed with brine and concentrated under reduced pressure onto silica. Purification (FCC, SiO2, 0-60%, EtOAc/hexanes) afforded the title compound as a white solid (1.0 g, 69%). 1H NMR (400 MHz, CDCl3) δ 9.44 (t, J=2.0 Hz, 1H), 9.00-8.94 (m, 1H), 8.88 (t, J=2.3 Hz, 1H), 7.74-7.65 (m, 1H), 7.47-7.33 (m, 1H), 7.28-7.26 (m, 1H), 7.21 (d, J=9.4 Hz, 1H), 7.07 (t, J=8.6 Hz, 1H), 5.25 (s, 2H), 4.59-4.38 (m, 2H), 1.52-1.41 (m, 3H). [M+H]=327.2.

Aufarbeitung

  1. customThe crude reaction mixture
  2. extractionThe aqueous later was extracted with EtOAc
  3. washthe combined organic fractions were washed with brine
  4. concentrationconcentrated under reduced pressure onto silica
  5. customPurification (FCC, SiO2, 0-60%, EtOAc/hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-282871b6f7bc47efbcd6b068af00f845
Quelldatensatz
uspto-grants-2015_08
Patentnummer
US09102674B2

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