Methanol → Exemestane

HRID 2065998

Reaktionsgleichung

Reaktionsgleichung von HRID 2065998
[CH2:1]=[C:2]1[C:19]2[C@:14]([CH3:21])([CH2:15][CH2:16][C:17](=[O:20])[CH:18]=2)[C@@H:13]2[C@H:4]([C@H:5]3[C@@:9]([CH2:11][CH2:12]2)([CH3:10])[C:8](=[O:22])[CH2:7][CH2:6]3)[CH2:3]1.C1(Cl)C(=O)C(Cl)=C(Cl)C(=O)C=1Cl.CO.CC(OC)(C)C>CN1CCCC1>[CH2:1]=[C:2]1[C:19]2[C@:14]([CH3:21])([CH:15]=[CH:16][C:17](=[O:20])[CH:18]=2)[C@@H:13]2[C@H:4]([C@H:5]3[C@@:9]([CH2:11][CH2:12]2)([CH3:10])[C:8](=[O:22])[CH2:7][CH2:6]3)[CH2:3]1

Komponenten

6

Edukt 4

HCID 887MethanolHCID 8371ChloranilHCID 15413tert-Butyl methyl etherHCID 129518006-Methylideneandrost-4-ene-3,17-dione

Produkt 1

HCID 60198ExemestaneAusbeute 60,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 84541-MethylpyrrolidineLösungsmittel

Reaktionsbedingungen

Temperatur
77.5 °C

Versuchsvorschrift

6-Methylen-androst-4-ene-3,17-dione (5.0 gm) was dissolved in N-methylpyrrolidine (25 mL) at RT & to it was charged Chloranil (12.37 gm) at RT. The reaction mass was heated to 75 to 80° C. for 18 hours. The progress of the reaction is monitored on TLC. The reaction mass was cooled down to room temperature and methanol was added to it. The reaction mass was stirred for next 30 minutes and precipitated solid mass was filtered through buchner funnel and washed with methanol. All the filtrates were combined and suitably diluted. The product from aqueous solution was extracted in toluene. Combined toluene extracts was washed with 2% aqueous NaOH solution under stirring for 30 minutes. The toluene layer was separated and washed with water. Toluene layer was dried over sodium sulfate, filtered and evaporated at reduced pressure to get solid residue. The solid residue was treated with MTBE to get 3.0 gm solid product. HPLC Purity: 97%.

Aufarbeitung

  1. temperatureThe reaction mass was cooled down to room temperature
  2. customprecipitated solid mass
  3. filtrationwas filtered through buchner funnel
  4. washwashed with methanol
  5. additionsuitably diluted
  6. extractionThe product from aqueous solution was extracted in toluene
  7. washCombined toluene extracts was washed with 2% aqueous NaOH solution
  8. stirringunder stirring for 30 minutes
  9. customThe toluene layer was separated
  10. washwashed with water
  11. dry with materialToluene layer was dried over sodium sulfate
  12. filtrationfiltered
  13. customevaporated at reduced pressure
  14. customto get solid residue

Quellen und Nachweise

ORD-Eintrag
ord-8871462b30404e98ae28401dc193bab5
Quelldatensatz
uspto-grants-2012_10
Patentnummer
US08288571B2

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