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1,2-Dimethoxyethane → 1,3-Dimethyl-7-(5,6-dihydroxyhexyl)xanthine

HRID 2290246
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HRID 2290246 반응식
Cl(O)(=O)(=O)=O.[CH3:6][N:7]1[C:16](=[O:17])[C:15]2[N:14]([CH2:18][CH2:19][CH2:20][CH2:21][CH:22]3[O:24][CH2:23]3)[CH:13]=[N:12][C:11]=2[N:10]([CH3:25])[C:8]1=[O:9].C[O:27]CCOC.C(=O)(O)[O-].[Na+]>O>[CH3:6][N:7]1[C:16](=[O:17])[C:15]2[N:14]([CH2:18][CH2:19][CH2:20][CH2:21][CH:22]([OH:24])[CH2:23][OH:27])[CH:13]=[N:12][C:11]=2[N:10]([CH3:25])[C:8]1=[O:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 80711,2-DimethoxyethaneHCID 24247Perchloric AcidHCID 516892Sodium BicarbonateHCID 131516391,3-Dimethyl-7-(5,6-epoxyhexyl)xanthine

생성물 1

HCID 131516061,3-Dimethyl-7-(5,6-dihydroxyhexyl)xanthine

시약·촉매·용매 1

HCID 962Water용매

실험 절차

0.24 ml of perchloric acid (70% strength) was added dropwise with stirring in 5 minutes to a solution of 3.6 g of 1,3-dimethyl-7-(5,6-epoxyhexyl)xanthine in 280 ml of a mixture of ethylene glycol dimethyl ether and water (volume ratio 3:2) at room temperature. After stirring at room temperature for 16 hours, the mixture was neutralized with sodium bicarbonate solution and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (mobile phase: chloroform/ethanol, volume ratio 8/2) and recrystallization from ethyl acetate.

후처리

  1. customevaporated under reduced pressure
  2. customThe residue was purified by column chromatography on silica gel (mobile phase: chloroform/ethanol, volume ratio 8/2) and recrystallization from ethyl acetate

출처 및 근거

ORD 기록
ord-0768ee77b848430ebe2d343af2d973af
출처 데이터셋
uspto-grants-1986_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04616020

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