반응 #367879

ord-f4e823ca4563425b917e2900a33a99d5

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The solvent was removed under vacuum
  2. 2
    기타the residue was partitioned between 100 mL of methylene chloride and 100 mL of 0.1N sodium hydroxide
  3. 3
    기타The organic layer was separated
  4. 4
    추출the aqueous layer was extracted with an additional 100 mL of methylene chloride
  5. 5
    세척washed with 100 mL of water
  6. 6
    건조dried (MgSO4)
  7. 7
    농축concentrated

실험 절차

To a solution of 2.76 g (0.01 mole) of 2,4-diamino-5-(3-hydroxy-4,5-dimethoxybenzyl)pyrimidine (D. E. Schwartz, W. Vetter, and G. Englert, Arzneim.-Forsch. (Drug Res.) 1970, 20, 1867; G. Rey-Bellet and R. Reiner, Helv. Chim. Acta 1970, 53, 945) in 40 mL of dry dimethyl sulfoxide was added 1.12 g (0.01 mole) of potassium t-butoxide. To the resulting suspension was added in one portion 1.16 g (0.0109 mole) of 3-chloro-2-butanone. The mixture was stirred at room temperature for 1 hour. The solvent was removed under vacuum and the residue was partitioned between 100 mL of methylene chloride and 100 mL of 0.1N sodium hydroxide. The organic layer was separated and the aqueous layer was extracted with an additional 100 mL of methylene chloride. The organic layers were combined, washed with 100 mL of water, dried (MgSO4) and concentrated to give a quantitative yield (3.58 g) of the title compound. Recrystallization from 95% ethanol gave an analytical sample; mp 167.5°-168.5°. Anal. Calc'd for C17H22N4O4 : C, 58.95; H, 6.40; N, 16.17. Found: C, 58.77; H, 6.42; N, 16.13.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04590271uspto-grants-1986_05