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Phosphorus oxychloride → 7-Chloro-6-iodothieno[3,2-b]pyridine

HRID 712013
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 712013
[I:1][C:2]1[C:3](O)=[C:4]2[S:10][CH:9]=[CH:8][C:5]2=[N:6][CH:7]=1.P(Cl)(Cl)([Cl:14])=O>>[Cl:14][C:3]1[C:2]([I:1])=[CH:7][N:6]=[C:5]2[CH:8]=[CH:9][S:10][C:4]=12
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 178516695HCID 178516695, Verbindung

Produkt 1

HCID 867174727-Chloro-6-iodothieno[3,2-b]pyridineAusbeute 44 %

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

A mixture of the crude 6-iodothieno[3,2-b]pyridin-7-ol (0.99 g, 3.6 mmol) in phosphoryl chloride (20 mL) was heated at 120° C. for 2 h. The reaction was cooled to room temperature, concentrated under reduced pressure. The residue was co-evaporated with toluene, then diluted with dichloromethane and neutralized carefully with sat. NaHCO3 solution. The black tar was filtered off and the filtrate was transferred to a separation funnel. The organic layer was concentrated and purified on silica gel (eluting with 0-35% EtOAc/hexanes) to give the desired product (44% in 2 steps). LCMS calculated for C7H4ClINS (M+H)+: m/z=295.9. Found: 295.8.

Aufarbeitung

  1. temperatureThe reaction was cooled to room temperature
  2. concentrationconcentrated under reduced pressure
  3. additiondiluted with dichloromethane and neutralized carefully with sat. NaHCO3 solution
  4. filtrationThe black tar was filtered off
  5. customthe filtrate was transferred to a separation funnel
  6. concentrationThe organic layer was concentrated
  7. custompurified on silica gel (eluting with 0-35% EtOAc/hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-23e3db47c5dc45aaab387cd855a348cb
Quelldatensatz
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09181271B2

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