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Water → 1-(9,10-dihydroxydecyl)-3,7-dimethylxanthine

HRID 1379013
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HRID 1379013 반응식
[CH2:1]([N:11]1[C:20](=[O:21])[C:19]2[N:18]([CH3:22])[CH:17]=[N:16][C:15]=2[N:14]([CH3:23])[C:12]1=[O:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH:9]=[CH2:10].C[N+]1([O-])CC[O:28]CC1.[OH2:32].S(S([O-])=O)([O-])=O.[Na+].[Na+]>C(O)(C)(C)C.CC(C)=O.[Os](=O)(=O)(=O)=O>[OH:32][CH:9]([CH2:10][OH:28])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][CH2:1][N:11]1[C:20](=[O:21])[C:19]2[N:18]([CH3:22])[CH:17]=[N:16][C:15]=2[N:14]([CH3:23])[C:12]1=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 962WaterHCID 24489Sodium DithioniteHCID 82029Methyl morpholine oxideHCID 15230636HCID 15230636, 화합물

생성물 1

HCID 98198951-(9,10-dihydroxydecyl)-3,7-dimethylxanthine수율 93%

시약·촉매·용매 3

HCID 6386tert-Butanol촉매
HCID 30318Osmium Tetroxide촉매
HCID 180Acetone용매

실험 절차

A solution of 1-(9-decenyl)-3,7-dimethylxanthine (CT1563) (3.2g, 10.1 mmol), 4-methylmorpholine-N-oxide (1.41 g, 12 mmol) and 2.5% osmium tetraoxide in t-butanol (3 drops) in acetone (40 ml) and water (10 ml) was stirred for 24 hr. After the addition of saturated sodium dithionite solution (5 ml) the mixture was stirred for 15 min. The mixture was extracted with 25% ethanol-dichloromethane (4×50 ml). The combined organic layers were dried over sodium sulfate and the solvents were evaporated under vacuum to a give solid which was recrystallized (ethanol) to give 1-(9,10-dihydroxydecyl)-3,7-dimethylxanthine (CT1564) (3.30 g, 93% yield).

후처리

  1. extractionThe mixture was extracted with 25% ethanol-dichloromethane (4×50 ml)
  2. dry with materialThe combined organic layers were dried over sodium sulfate
  3. customthe solvents were evaporated under vacuum to a give solid which
  4. customwas recrystallized (ethanol)

출처 및 근거

ORD 기록
ord-a0e33d7e03e6441fb5fe7a16f7e53dae
출처 데이터셋
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05670506

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