تفاعل #10530

ord-69e4a8157db7424a83d31d8e7356ee4a

معادلة التفاعل

C1=COCCC1
3,4-dihydro-2H-pyran
Clc1nc(Cl)c2nc[nH]c2n1
2,6-Dichloro-9H-purine
Cc1ccc(S(=O)(=O)O)cc1.O
4-toluenesulphonic acid monohydrate
O=C([O-])O.[Na+]
sodium hydrogen carbonate
Clc1nc(Cl)c2ncn(C3CCCCO3)c2n1
title compound
Clc1nc(Cl)c2ncn(C3CCCCO3)c2n1
2,6-Dichloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine

ظروف التفاعل

درجة الحرارة
50°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction mixture was cooled to room temperature
  2. 2
    أخرىThe organic layer was separated
  3. 3
    غسيلwashed sequentially with water and brine
  4. 4
    تجفيفdried over anhydrous magnesium sulphate
  5. 5
    ترشيحfiltered
  6. 6
    أخرىthe solvent removed under reduced pressure
  7. 7
    أخرىThe residue was azeotroped with pentane (×2)

الإجراء التجريبي

2,6-Dichloro-9H-purine (20 g, 0.11 mol) and 4-toluenesulphonic acid monohydrate (0.2 g) were dissolved in ethyl acetate (300 ml), the mixture heated to 50° C. and a solution of 3,4-dihydro-2H-pyran (12.6 ml, 0.14 mol) in ethyl acetate (50 ml) added slowly over 30 minutes. The reaction mixture was cooled to room temperature, water (100 ml) added and the pH of the solution adjusted to 7 by addition of a saturated aqueous solution of sodium hydrogen carbonate. The organic layer was separated, washed sequentially with water and brine, dried over anhydrous magnesium sulphate, filtered and the solvent removed under reduced pressure. The residue was azeotroped with pentane (×2) to afford the title compound as a slightly impure white solid (30.9 g).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07094769B2uspto-grants-2006_08