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1,1',1''-(Chlorosilylidyne)tris(benzene) → HCID 178420877, 화합물

HRID 724798
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인쇄 미리보기

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HRID 724798 반응식
Cl[C:2]1[N:10]=[CH:9][N:8]=[C:7]2[C:3]=1[N:4]=[CH:5][N:6]2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O.C1([Si](C2C=CC=CC=2)(C2C=CC=CC=2)Cl)C=CC=CC=1>N1C=CC=CC=1>[N:10]1[CH:2]=[C:3]2[C:7]([NH:6][CH:5]=[N:4]2)=[N:8][CH:9]=1
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참가 물질

4

반응물 2

HCID 64581,1',1''-(Chlorosilylidyne)tris(benzene)HCID 930036-Chloropurine riboside

생성물 1

HCID 178420877HCID 178420877, 화합물

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

14.3 g of 6-chloro-9-β-D-ribofuranosyl-9H-purine and 15 g of triphenylchlorosilane were dissolved in 500 ml of pyridine and stirred for one hour at room temperature. Pyridine was distilled away and the residue was dissolved in benzene. The benzene layer was washed with 1N HCl and brine, and then dried over sodium sulfate anhydride. The solvent was distilled off and the residue was recrystallized from a mixture of hexane and ethyl acetate to give 21.5 g of 6-chloro-9-15-O-triphenylsilyl-β-D-ribofuranosyl)-9H-purine.

후처리

  1. distillationPyridine was distilled away
  2. dissolutionthe residue was dissolved in benzene
  3. washThe benzene layer was washed with 1N HCl and brine
  4. dry with materialdried over sodium sulfate anhydride
  5. distillationThe solvent was distilled off
  6. customthe residue was recrystallized from a mixture of hexane and ethyl acetate

출처 및 근거

ORD 기록
ord-1b1fd65bc36e4302b62143f7095a7269
출처 데이터셋
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05705491

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