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Trifluoroacetic acid → 2-(5-Chloro-2,4-difluorophenyl)pyridin-4-amine

HRID 1522548
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1522548
Br[C:2]1[CH:7]=[C:6]([NH:8]C(=O)OC(C)(C)C)[CH:5]=[CH:4][N:3]=1.[Cl:16][C:17]1[C:18]([F:27])=[CH:19][C:20]([F:26])=[C:21](B(O)O)[CH:22]=1.C([O-])([O-])=O.[Na+].[Na+].FC(F)(F)C(O)=O>O1CCOCC1.ClCCl.[Pd](Cl)Cl.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.O>[Cl:16][C:17]1[C:18]([F:27])=[CH:19][C:20]([F:26])=[C:21]([C:2]2[CH:7]=[C:6]([NH2:8])[CH:5]=[CH:4][N:3]=2)[CH:22]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 4

HCID 6422Trifluoroacetic acidHCID 10340Sodium CarbonateHCID 3769192(5-Chloro-2,4-difluorophenyl)boronic acidHCID 70155224-(Boc-amino)-2-bromopyridine

Produkt 1

HCID 674696122-(5-Chloro-2,4-difluorophenyl)pyridin-4-amineAusbeute 21,5 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 6102075
Dichlorobis(triphenylphosphine)palladium
Katalysator
HCID 962WaterLösungsmittel
HCID 6344DichloromethaneLösungsmittel
HCID 312751,4-DioxaneLösungsmittel

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

tert-Butyl 2-bromopyridin-4-ylcarbamate (258 mg, 0.945 mmol), 5-chloro-2,4-difluorophenylboronic acid (236 mg, 1.228 mmol) and bis(triphenylphosphine) palladium chloride (133 mg, 0.189 mmol) were combined in dioxane (5 mL) and saturated Na2CO3 (0.472 ml, 0.945 mmol). The reaction mixture was heated at 90° C. in an oil bath. After 12 hours, the reaction mixture was cooled, water (10 mL) was added and the reaction mixture was extracted with EtOAc (100 mL, 2×). The organic layers were combined, washed with brine, dried over Na2SO4, filtered, and concentrated to give a residue. The residue was dissolved in dichloromethane (4 mL) and trifluoroacetic acid was added (4 mL). The reaction was stirred at room temperature for 20 minutes then the solvent was removed on a rotavap and the residue was further dried under high vacuum overnight. This residue was purified by NH column chromatography, eluted with EtOAc in Hexanes (0-100%) to give the title compound (49 mg) as white solid. ESI-MS: m/z 242.0 (M+H).

Aufarbeitung

  1. temperaturethe reaction mixture was cooled
  2. extractionthe reaction mixture was extracted with EtOAc (100 mL, 2×)
  3. washwashed with brine
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto give a residue
  8. customthe solvent was removed on a rotavap
  9. customthe residue was further dried under high vacuum overnight
  10. customThis residue was purified by NH column chromatography
  11. washeluted with EtOAc in Hexanes (0-100%)

Quellen und Nachweise

ORD-Eintrag
ord-ccee064e0c5e42d7b99cb1181d9941db
Quelldatensatz
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09073918B2

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