Hydrochloric Acid → 3-methyl-1-(1-methylethyl)-6-(methyloxy)-1H-indole-4-carboxylic acid

HRID 593900Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 593900
Br[C:2]1[CH:3]=[C:4]([C:15]([O:17]C)=[O:16])[C:5]2[C:6]([CH3:14])=[CH:7][N:8]([CH:11]([CH3:13])[CH3:12])[C:9]=2[CH:10]=1.[CH3:19][O-:20].[Na+].CO.Cl>O.CCOC(C)=O.[Cu]I.CN1C(=O)CCC1>[CH3:14][C:6]1[C:5]2[C:4]([C:15]([OH:17])=[O:16])=[CH:3][C:2]([O:20][CH3:19])=[CH:10][C:9]=2[N:8]([CH:11]([CH3:12])[CH3:13])[CH:7]=1

Komponenten

9

Edukt 4

HCID 313Hydrochloric AcidHCID 887MethanolHCID 10942334Sodium MethoxideHCID 67464634methyl 6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxylate

Produkt 1

HCID 674653313-methyl-1-(1-methylethyl)-6-(methyloxy)-1H-indole-4-carboxylic acidAusbeute 80 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)KatalysatorHCID 962WaterLösungsmittel2×HCID 8857Ethyl AcetateLösungsmittelHCID 13387N-methyl-2-pyrrolidoneLösungsmittel

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

To methyl 6-bromo-3-methyl-1-(1-methylethyl)-1H-indole-4-carboxylate (1.3 g, 4.19 mmol) and copper(I) iodide (1.0 g, 5.25 mmol) was added NMP (8 mL). To the mixture was added dropwise a solution of sodium methoxide 25 wt % in methanol (4.0 mL, 17.49 mmol) with stirring. The reaction was heated to 120° C. and stirred for 1.5 hr. The reaction was allowed to cool and when the temperature reached 80° C., water (200 uL) was added. The reaction was allowed to continue to cool to RT and stirred overnight. The reaction was acidified with 1N HCl (17 mL) and diluted with water and EtOAc. The mixture was filtered through Celite and washed with EtOAc. The filtrate was poured into a separatory funnel and the organic phase was separated, washed with brine, dried (MgSO4), filtered, and concentrated under vacuum. Purification by silica gel chromatography (Analogix, SF25-60g, 20 to 50% EtOAc in hexanes) gave after concentration, trituration with hexanes, filtration and drying under vacuum 3-methyl-1-(1-methylethyl)-6-(methyloxy)-1H-indole-4-carboxylic acid (825 mg, 3.34 mmol, 80% yield) as an light yellow solid. MS(ES)+ m/e 248.3 [M+H]+.

Aufarbeitung

  1. stirringstirred for 1.5 hr
  2. temperatureto cool
  3. customreached 80° C.
  4. temperatureto cool to RT
  5. stirringstirred overnight
  6. filtrationThe mixture was filtered through Celite
  7. washwashed with EtOAc
  8. additionThe filtrate was poured into a separatory funnel
  9. customthe organic phase was separated
  10. washwashed with brine
  11. dry with materialdried (MgSO4)
  12. filtrationfiltered
  13. concentrationconcentrated under vacuum
  14. customPurification by silica gel chromatography (Analogix, SF25-60g, 20 to 50% EtOAc in hexanes)
  15. customgave
  16. concentrationafter concentration, trituration
  17. filtrationwith hexanes, filtration

Quellen und Nachweise

ORD-Eintrag
ord-191d403d041d4b27a2130e31ddbab3f0
Quelldatensatz
uspto-grants-2016_01
Patentnummer
US09242962B2

Notizen zur Reaktion

Wird geladen…