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Hydrochloric Acid → N-(5-bromo-2-chloropyridin-3-yl)-4-fluorobenzenesulfonamide

HRID 1162444
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1162444
[NH2:1][C:2]1[C:3]([Cl:9])=[N:4][CH:5]=[C:6]([Br:8])[CH:7]=1.N1C=CC=CC=1.[F:16][C:17]1[CH:22]=[CH:21][C:20]([S:23](Cl)(=[O:25])=[O:24])=[CH:19][CH:18]=1.C(=O)([O-])[O-].[K+].[K+].Cl>O.O1CCOCC1.CO>[Br:8][C:6]1[CH:7]=[C:2]([NH:1][S:23]([C:20]2[CH:21]=[CH:22][C:17]([F:16])=[CH:18][CH:19]=2)(=[O:25])=[O:24])[C:3]([Cl:9])=[N:4][CH:5]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 5

HCID 313Hydrochloric AcidHCID 1049PyridineHCID 95884-Fluorobenzenesulfonyl chlorideHCID 11430Potassium CarbonateHCID 218583543-Amino-5-bromo-2-chloropyridine

Produkt 1

HCID 53363354N-(5-bromo-2-chloropyridin-3-yl)-4-fluorobenzenesulfonamide
Ausbeute 60,4 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 887MethanolLösungsmittelHCID 962WaterLösungsmittelHCID 312751,4-DioxaneLösungsmittel

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

To a 50-mL, round-bottomed flask was added 3-amino-5-bromo-2-chloropyridine (0.50 g, 2.4 mmol, Asymchem, Morrisville, N.C.), pyridine (10 mL, 120 mmol) and 4-fluorobenzenesulfonyl chloride (2.0 g, 10 mmol, Fluka, Buchs, Switzerland). The mixture was stirred at 25° C. After 18 hours, the mixture was concentrated in vacuo. To the residue was added methanol (10 mL), 1,4-dioxane (10 mL) and potassium carbonate (3.4 g, 25 mmol). The mixture was stirred at 60° C. After 16 hours, the mixture was poured into water (100 mL) and the pH was adjusted to ˜7 with 1 N HCl. The solution was extracted with EtOAc (3×75 mL) and the combined extracts were washed with water (100 mL), brine (100 mL) and then dried (Na2SO4) and concentrated onto silica. Purification by silica gel chromatography (2.0 to 30% EtOAc/hexane) afforded the title compound as a white solid (0.53 g, 58% yield). MS (ESI pos. ion) m/z: 367 (M+1). 1H NMR (400 MHz, DMSO-d6) δ ppm 10.63 (br. s, 1H), 8.42 (d, J=2.3 Hz, 1H), 7.94 (d, J=2.3 Hz, 1H), 7.77-7.84 (m, 2H), 7.40-7.47 (m, 2H).

Aufarbeitung

  1. concentrationthe mixture was concentrated in vacuo
  2. stirringThe mixture was stirred at 60° C
  3. waitAfter 16 hours
  4. extractionThe solution was extracted with EtOAc (3×75 mL)
  5. washthe combined extracts were washed with water (100 mL), brine (100 mL)
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated onto silica
  8. customPurification by silica gel chromatography (2.0 to 30% EtOAc/hexane)

Quellen und Nachweise

ORD-Eintrag
ord-ae39fcef37e34a83b01f71b8ef40027b
Quelldatensatz
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07820665B2

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