반응 #62718

ord-79c9ecf8ec8c48b79a4125b9f9a1d2ef

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The mixture was heated at 65° overnight
  2. 2
    기타The solvent was removed under vacuum
  3. 3
    기타the residue was partitioned between 750 mL methylene chloride and 750 mL of 0.1N sodium hydroxide
  4. 4
    기타The organic layer was separated
  5. 5
    추출the aqueous layer was extracted with an additional 750 mL of methylene chloride
  6. 6
    세척washed with 750 mL of water
  7. 7
    건조dried (MgSO4)
  8. 8
    기타purified by flash column chromatography

실험 절차

To a solution of 27.6 g, (0.1 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 400 mL of dry dimethyl sulfoxide was added 11.22 g (0.10 mole) of potassium t-butoxide. To the resulting suspension was added dropwise 17.92 g (0.107 mole) of β-chloropropionaldehyde diethylacetal. The mixture was heated at 65° overnight. The solvent was removed under vacuum and the residue was partitioned between 750 mL methylene chloride and 750 mL of 0.1N sodium hydroxide. The organic layer was separated and the aqueous layer was extracted with an additional 750 mL of methylene chloride. The organic layers were combined, washed with 750 mL of water, dried (MgSO4), and purified by flash column chromatography to yield 33.38 g (83%) of the title compound (mp 105°-106.5° ). Anal. Calcd for C20H30N4O5 : C, 59.10; H, 7.44; N, 13.78. Found: C, 58.71; H, 7.40; N, 13.58.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04761475uspto-grants-1988_08