Methane → HCID 18465367, 화합물

HRID 437537

반응식

HRID 437537 반응식
[CH2:1]([N:4]1[C:13](=[O:14])[C:12]2[NH:11][CH:10]=[N:9][C:8]=2[N:7]([CH2:15][CH2:16][CH3:17])[C:5]1=[O:6])[CH2:2][CH3:3].[OH-].[Na+].Cl[CH2:21][CH:22]([OH:25])[CH2:23][OH:24].C>O.C(O)(C)C.C(Cl)(Cl)Cl.CO>[OH:25][CH:22]([CH2:23][OH:24])[CH2:21][N:11]1[C:12]2[C:13](=[O:14])[N:4]([CH2:1][CH2:2][CH3:3])[C:5](=[O:6])[N:7]([CH2:15][CH2:16][CH3:17])[C:8]=2[N:9]=[CH:10]1

참가 물질

8

실험 절차

A suspension of 1,3-di-n-propylxanthine (250.1 g., 1.06 mole) in water (300 ml.) was treated with sodium hydroxide solution (50%, 85 ml.). The mixture was filtered, and evaporated to dryness. The residue obtained was treated with a solution of 1-chloro-2,3-dihydroxypropane (170 g., 1.59 mole) in isopropanol (700 ml.). The mixture was stirred at reflux overnight, filtered, and evaporated to dryness to obtain a brown gummy residue. This residue was dissolved in isopropyl alcohol, and stirred overnight with charcoal (20 gm.). The mixture was filtered, concentrated and allowed to crystallize over night at 0° to -5° C. The crystals were filtered, suspended in ether, refiltered and air dried to yield white crystals (224 g., 72.17%), melting point 88° - 91°. Tlc (5μl of a 5% solution) on a silica plate developed in chloroform:methanol (9.5:0.5) showed one spot. IR and NMR spectra were consistent with the proposed structure.

후처리

  1. filtrationThe mixture was filtered
  2. customevaporated to dryness
  3. customThe residue obtained
  4. temperatureat reflux overnight
  5. filtrationfiltered
  6. customevaporated to dryness
  7. customto obtain a brown gummy residue
  8. filtrationThe mixture was filtered
  9. concentrationconcentrated
  10. customto crystallize over night at 0° to -5° C
  11. filtrationThe crystals were filtered
  12. customair dried
  13. customto yield white crystals (224 g., 72.17%), melting point 88° - 91°

출처 및 근거

ORD 기록
ord-416bfc39d5184c4ca3f8be7fd02d440f
출처 데이터셋
uspto-grants-1977_06
특허 번호
US04031218

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