5-bromo-6-fluoro-2,3-dihydro-1H-indole-7-carboxylic acid → 5-bromo-6-fluoro-1H-indole-7-carboxylic acid

HRID 656067Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 656067
[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([C:12]([OH:14])=[O:13])[C:10]=1[F:11])[NH:7][CH2:6][CH2:5]2>C1COCC1.Cl.O=[Mn]=O>[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([C:12]([OH:14])=[O:13])[C:10]=1[F:11])[NH:7][CH:6]=[CH:5]2

Komponenten

5

Edukt 1

HCID 593326645-bromo-6-fluoro-2,3-dihydro-1H-indole-7-carboxylic acid

Produkt 1

HCID 593327305-bromo-6-fluoro-1H-indole-7-carboxylic acidAusbeute 61,7 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 14801Manganese dioxideKatalysatorHCID 313Hydrochloric AcidLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a stirred solution of 5-bromo-6-fluoro-2,3-dihydro-1H-indole-7-carboxylic acid (5.8 g, 0.022 mol) in THF (120 mL) was added MnO2 (11.6 g, 0.134 mol). The reaction mixture was stirred at reflux overnight and then filtered (hot) through celite, washing with hot THF (2×75 mL). The filtrate was concentrated, giving a brown solid, which was suspended in 1M HCl (150 mL). The mixture stirred at reflux overnight to remove traces of Mn and then cooled to room temperature. The solid was filtered off, dried, and recrystallised from IPA, giving 3.5 g (61%) of the title compound.

Aufarbeitung

  1. temperatureat reflux overnight
  2. filtrationfiltered (hot) through celite
  3. washwashing with hot THF (2×75 mL)
  4. concentrationThe filtrate was concentrated
  5. customgiving a brown solid, which
  6. stirringThe mixture stirred
  7. temperatureat reflux overnight
  8. customto remove traces of Mn
  9. filtrationThe solid was filtered off
  10. customdried
  11. customrecrystallised from IPA

Quellen und Nachweise

ORD-Eintrag
ord-5925b50d9a064015900ea213439de480
Quelldatensatz
uspto-grants-2011_12
Patentnummer
US08071584B2

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