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Potassium Hydroxide → 8-(2-Methoxy-4-benzyloxy-phenyl)-2-benzyloxypurine

HRID 3870
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인쇄 미리보기

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HRID 3870 반응식
[OH-:1].[K+].[CH3:3][O:4][C:5]1[CH:10]=[C:9]([O:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:8]=[CH:7][C:6]=1[C:19]1[NH:27][C:26]2[C:21](=[N:22][C:23](Cl)=[N:24][CH:25]=2)[N:20]=1>C(O)C1C=CC=CC=1>[CH3:3][O:4][C:5]1[CH:10]=[C:9]([O:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:8]=[CH:7][C:6]=1[C:19]1[NH:27][C:26]2[C:21](=[N:22][C:23]([O:1][CH2:19][C:6]3[CH:7]=[CH:8][CH:9]=[CH:10][CH:5]=3)=[N:24][CH:25]=2)[N:20]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 135323868-(2-Methoxy-4-benzyloxy-phenyl)-2-chloro-purine

생성물 1

HCID 135323998-(2-Methoxy-4-benzyloxy-phenyl)-2-benzyloxypurine

시약·촉매·용매 1

HCID 244Benzyl Alcohol용매

반응 조건

온도
150 °C

실험 절차

An amount of 4.5 gm of powdered potassium hydroxide is dissolved in 70 ml of benzyl alcohol, and then 7.2 gm of 8-(2-methoxy-4-benzyloxy-phenyl)-2-chloro-purine are added. The mixture is heated to 150° C. for three hours, cooled, and filtered, the filtrate is mixed with ether, and the precipitate obtained is purified by chromatography on silica gel [eluant: methylene chloride/ethanol (100:2.5)].

후처리

  1. temperaturecooled
  2. filtrationfiltered
  3. additionthe filtrate is mixed with ether
  4. customthe precipitate obtained
  5. customis purified by chromatography on silica gel [eluant: methylene chloride/ethanol (100:2.5)]

출처 및 근거

ORD 기록
ord-18a6059416844248a8ba411c923fd244
출처 데이터셋
uspto-grants-1988_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04722929

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