Bromine → HCID 20144337, 화합물

HRID 648940

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HRID 648940 반응식
[Br:1]Br.[O:3]=[C:4]([CH3:22])[CH2:5][CH2:6][CH2:7][CH2:8][N:9]1[C:17]2[C:16](=[O:18])[N:15]([CH3:19])[C:14](=[O:20])[N:13]([CH3:21])[C:12]=2[N:11]=[CH:10]1.[Na]>CO.O>[Br:1][CH2:22][C:4](=[O:3])[CH2:5][CH2:6][CH2:7][CH2:8][N:9]1[C:17]2[C:16](=[O:18])[N:15]([CH3:19])[C:14](=[O:20])[N:13]([CH3:21])[C:12]=2[N:11]=[CH:10]1

참가 물질

6

실험 절차

9.7 Grams (0.06 moles) of bromine were added to a solution of 15 g (0.054 moles) of 7-(5-keto-hexyl)-1,3-dimethylxanthine in 100 ml of anhydrous methanol, at 10° C. with stirring. After 30 minutes at the same temperature, stirring was continued for 7 more hours at room temperature. The mixture was then concentrated under reduced pressure till a residual volume of 30 ml, diluted with 30 ml of water, added with 3 drops of 96% sulphuric acid and stirred for 4 hours at room temperature, to hydrolyze any dimethylketal formed, then diluted with 100 ml of water and alkalized with a 10% sodium bicarbonte aqueous solution. The mixture was extracted with 2×80 ml of methylene chloride, the organic phase was washed with water, dried and evaporated under reduced pressure. The residue was dissolved in 30 ml of ethyl acetate, cooled and crystallized at 5°-10° C. 7.5 Grams (40%) of the title compound were obtained, melting at 106°-109° C., which was directly used in the next step.

후처리

  1. stirringstirring
  2. customwas continued for 7 more hours at room temperature
  3. concentrationThe mixture was then concentrated under reduced pressure till a residual volume of 30 ml
  4. additiondiluted with 30 ml of water
  5. additionadded with 3 drops of 96% sulphuric acid
  6. stirringstirred for 4 hours at room temperature
  7. customformed
  8. extractionThe mixture was extracted with 2×80 ml of methylene chloride
  9. washthe organic phase was washed with water
  10. customdried
  11. customevaporated under reduced pressure
  12. dissolutionThe residue was dissolved in 30 ml of ethyl acetate
  13. temperaturecooled
  14. customcrystallized at 5°-10° C

출처 및 근거

ORD 기록
ord-cc8e4b5122b04b76a84f77478a2a009e
출처 데이터셋
uspto-grants-1988_04
특허 번호
US04737502

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