Reaktion #336977

ord-6621c962023f47de9655ad5bd540ffe3

Reaktionsgleichung

Clc1nc(Cl)c2[nH]cnc2n1
2,6-dichloropurine
C1=COCCC1
dihydropyran
CC1(C)[C@@H]2CC[C@@]1(CS(=O)(=O)O)C(=O)C2
D-(+)-10-camphorsulfonic acid
Clc1nc(Cl)c2ncn(C3CCCCO3)c2n1
desired product
Clc1nc(Cl)c2ncn(C3CCCCO3)c2n1
2,6-dichloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine

Reaktionsbedingungen

Temperatur
83°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.WAITThe initially white suspension, after 2 hrs
  2. 2
    Waschenwashed with brine
  3. 3
    TrocknenThe organic layer is dried over MgSO4
  4. 4
    Filtrationfiltered
  5. 5
    Einengenconcentrated
  6. 6
    Sonstigetriturated with hexane 3 times

Vorschrift

A suspension of 2,6-dichloropurine (22.0 g, 116.4 mmol), dihydropyran (11.5 mL, 126 mmol) and D-(+)-10-camphorsulfonic acid (2.20 g, 9.47 mmol) in 1,2-dichloroethane (300 mL) was stirred at 83° C. for 16 hours. The initially white suspension, after 2 hrs, turned yellow and then black. The reaction mixture was diluted with CCl3H and then washed with brine. The organic layer is dried over MgSO4, filtered, concentrated and triturated with hexane 3 times to give the desired product. 1HNMR (300 MHz, CCl3D): δ 8.33 (s, 1H), 5.75 (dd, J=10.4 Hz, 2.5 Hz, 1H), 4.18 (m, 2H), 3.79 (m, 2H), 1.84 (m, 4H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07863285B2uspto-grants-2011_01