Sodium Sulfate → 7-Fluorotryptamine

HRID 1371969Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1371969
[H-].[Al+3].[Li+].[H-].[H-].[H-].[F:7][C:8]1[CH:9]=[CH:10][CH:11]=[C:12]2[C:16]=1[NH:15][CH:14]=[C:13]2[CH:17]=[CH:18][N+:19]([O-])=O.S([O-])([O-])(=O)=O.[Na+].[Na+]>C1COCC1>[F:7][C:8]1[CH:9]=[CH:10][CH:11]=[C:12]2[C:16]=1[NH:15][CH:14]=[C:13]2[CH2:17][CH2:18][NH2:19]

Komponenten

5

Versuchsvorschrift

Combine lithium aluminum hydride (12.8 g; 336.1 mmol) and 0° C. anhydrous tetrahydrofuran (160 mL). Cool resulting exotherm to 0° C. Add 7-fluoro-3-(2-nitrovinyl)-1H-indole (11.55 g, 56.0 mmol) in anhydrous THF (200 mL) dropwise. After 30 min, warm to ambient temperature. After 4 hours, cool to 0° C. and add saturated sodium sulfate solution (35 mL) dropwise. Filter the solids and wash with THF and ethyl acetate. Concentrate the filtrate and dissolve the residue in methylene chloride. Filter the precipitate to give 1.26 g of product as brown crystals. Concentrate the filtrate and chromatograph on silica gel eluting with 5%, 7%, 10% 2N ammonia in methanol/methylene chloride to give product: MS(m/e): 179 (M+1), 177 (M−1); Calculated for C10H11FN2: Calcd: C, 67.40; H, 6.22; N, 15.72. Found: C, 67.06; H, 6.11; N, 15.48.

Aufarbeitung

  1. temperatureCool
  2. customresulting exotherm to 0° C
  3. waitAfter 4 hours
  4. temperaturecool to 0° C.
  5. filtrationFilter the solids
  6. washwash with THF and ethyl acetate
  7. concentrationConcentrate the filtrate
  8. dissolutiondissolve the residue in methylene chloride
  9. filtrationFilter the precipitate

Quellen und Nachweise

ORD-Eintrag
ord-76972c4762344498869c8584040afedf
Quelldatensatz
uspto-grants-2007_01
Patentnummer
US07157488B2

Notizen zur Reaktion

Wird geladen…