Methanol → Famciclovir

HRID 393386

Reaktionsgleichung

Reaktionsgleichung von HRID 393386
Cl.[NH2:2][C:3]1[N:11]=[C:10]2[C:6]([N:7]=[CH:8][N:9]2[CH2:12][CH2:13][CH:14]([CH2:17][OH:18])[CH2:15][OH:16])=[CH:5][N:4]=1.C(N([CH2:24][CH3:25])CC)C.[C:26](OC(=O)C)(=[O:28])[CH3:27].C[OH:34]>CN(C)C1C=CN=CC=1.ClCCl.CC(O)C>[C:26]([O:16][CH2:15][CH:14]([CH2:17][O:18][C:24](=[O:34])[CH3:25])[CH2:13][CH2:12][N:9]1[CH:8]=[N:7][C:6]2[C:10]1=[N:11][C:3]([NH2:2])=[N:4][CH:5]=2)(=[O:28])[CH3:27]

Komponenten

8

Edukt 4

HCID 887MethanolHCID 7918Acetic AnhydrideHCID 8471TriethylamineHCID 44226540Desacetyl famciclovir hydrochloride

Produkt 1

HCID 3324FamciclovirAusbeute 70 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 142844-(Dimethylamino)pyridineKatalysatorHCID 3776IsopropanolLösungsmittelHCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a stirred suspension of 2-amino-9-(4-hydroxy-3-hydroxymethylbut-1-yl)purine hydrochloride (0.79 g), 4-dimethylaminopyridine (16 mg) and triethylamine (1.4 ml) in dichloromethane (16 ml) at room temperature was added acetic anhydride (0.57 ml). The resulting mixture was stirred at ambient temperature for 2.25 hours. Methanol (4 ml) was added and the solution stirred for 0.5 hours before being evaporated to dryness. Water (20 ml) was added and the aqueous solution extracted with dichloromethane (3×20 ml). The combined extracts were concentrated to give an oil. This oil was dissolved in 2-propanol (5 ml), the solvent evaporated and the residue recrystallised from 2-propanol (5 ml). The product was collected by filtration, washed with 2-propanol (3 ml) and dried to give the title compound (654 mg, 70%).

Aufarbeitung

  1. stirringthe solution stirred for 0.5 hours
  2. custombefore being evaporated to dryness
  3. additionWater (20 ml) was added
  4. extractionthe aqueous solution extracted with dichloromethane (3×20 ml)
  5. concentrationThe combined extracts were concentrated
  6. customto give an oil
  7. customthe solvent evaporated
  8. customthe residue recrystallised from 2-propanol (5 ml)
  9. filtrationThe product was collected by filtration
  10. washwashed with 2-propanol (3 ml)
  11. customdried

Quellen und Nachweise

ORD-Eintrag
ord-9ad1f9c441df42e1884e9625e9eeaff8
Quelldatensatz
uspto-grants-2004_10
Patentnummer
US06806375B2

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