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Water → HCID 53812209, 화합물

HRID 361490
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HRID 361490 반응식
[NH:1]1[C:12](=[O:13])[C:11]2[N:9]([CH3:10])[CH:8]=[N:7][C:6]=2[N:4]([CH3:5])[C:2]1=[O:3].[H-].[Na+].CS(O[CH2:21][CH2:22][CH2:23][CH:24]=[CH:25][CH3:26])(=O)=O.O>CS(C)=O>[CH2:26]([N:1]1[C:12](=[O:13])[C:11]2[N:9]([CH3:10])[CH:8]=[N:7][C:6]=2[N:4]([CH3:5])[C:2]1=[O:3])[CH2:25][CH2:24][CH:23]=[CH:22][CH3:21]
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참가 물질

6

반응물 4

HCID 962WaterHCID 5429TheobromineHCID 24758Sodium hydrideHCID 54547883HCID 54547883, 화합물

생성물 1

HCID 53812209HCID 53812209, 화합물수율 67%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

A mixture of theobromine (2.16 g, 12 mmol) and sodium hydride (288 mg, 12 mequivalents) in dimethylsufoxide (10 mL) was stirred for 30 minutes and then a solution of 1-methansulfonyloxy-4-hexene in dimethylsulfoxide (10 mL) was added. After 84 hours of stirring, water (70 mL) is added and the mixture extracted with ether (3×50 mL). The combined extracts were washed with water (50 mL) and dried over magnesium sulfate. The solvent was then evaporated under vacuum. The residue was purified by flash chromatography (22 g silica gel using an ethyl acetate eluant, 500 mL), yielding 2.1 g (67%) 1-(4-hexenyl)-3,7-dimethylxanthine. To a solution of 1-(4-hexenyl)-3,7-dimethylxanthine (270 mg, 1.03 mmol) in dichloromethane (10 mL) was added saturated aqueous sodium bicarbonate solution (10 mL), followed by a solution of 50-60% 3-chloroperoxybenzoic acid (889 mg, 2.58 mmol) in dichloromethane (5 mL) over 1 minute. After 20 hours of stirring, 20% aqueous sodium metabisulfite solution (15 mL) was added over 1 minute. The mixture was then extracted with dichloromethane (3×15 mL). The combined extracts were washed with saturated aqueous sodium bicarbonate solution (3×20 mL) and dried over magnesium sulfate. The sovent was evaporated under vacuum. The residue was purified by flash chromatography using 14 g of silica gel and eluting with ethyl acetate (100 ml) followed by 8% methanol-dichloromethane (60 mL), yielding 80 mg (28% yield) of 1-(4,5-oxohexyl)-3,7-dimethylxanthine as a white powder.

후처리

  1. stirringAfter 84 hours of stirring
  2. extractionthe mixture extracted with ether (3×50 mL)
  3. washThe combined extracts were washed with water (50 mL)
  4. dry with materialdried over magnesium sulfate
  5. customThe solvent was then evaporated under vacuum
  6. customThe residue was purified by flash chromatography (22 g silica gel using an ethyl acetate eluant, 500 mL),

출처 및 근거

ORD 기록
ord-f90bb52d5a244d5c9607cd370f5bfb55
출처 데이터셋
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05866576

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