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Acetone → (2S,3S,4R,5R)-5-(6-[(2,2-Diphenylethyl)amino]-2-{[({[2-(1-piperidinyl)ethyl]amino}carbonyl)amino]methyl}-9H-purin-9-yl)-N-ethyl-3,4-dihydroxytetrahydro-2-furancarboxamide

HRID 897075
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HRID 897075 반응식
C(=O)([O-])[O-].[K+].[K+].C([O:15][C@H:16]1[C@@H:20]([O:21]C(=O)C2C=CC=CC=2)[C@H:19]([N:30]2[CH:38]=[N:37][C:36]3[C:31]2=[N:32][C:33]([CH2:54][NH:55][C:56]([NH:58][CH2:59][CH2:60][N:61]2[CH2:66][CH2:65][CH2:64][CH2:63][CH2:62]2)=[O:57])=[N:34][C:35]=3[NH:39][CH2:40][CH:41]([C:48]2[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=2)[C:42]2[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=2)[O:18][C@@H:17]1[C:67]([NH:69][CH2:70][CH3:71])=[O:68])(=O)C1C=CC=CC=1.CC(C)=O>CO>[C:42]1([CH:41]([C:48]2[CH:49]=[CH:50][CH:51]=[CH:52][CH:53]=2)[CH2:40][NH:39][C:35]2[N:34]=[C:33]([CH2:54][NH:55][C:56]([NH:58][CH2:59][CH2:60][N:61]3[CH2:66][CH2:65][CH2:64][CH2:63][CH2:62]3)=[O:57])[N:32]=[C:31]3[C:36]=2[N:37]=[CH:38][N:30]3[C@@H:19]2[O:18][C@H:17]([C:67]([NH:69][CH2:70][CH3:71])=[O:68])[C@@H:16]([OH:15])[C@H:20]2[OH:21])[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1
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참가 물질

5

반응물 3

HCID 180AcetoneHCID 11430Potassium Carbonate2회HCID 58904390(2S,3S,4R,5R)-4-(Benzoyloxy)-5-(6-[(2,2-diphenylethyl)amino]-2-{[({[2-(1-piperidinyl) ethyl]amino}carbonyl)amino]methyl}-9H-Purin-9-yl)-2-[(ethylamino)carbonyl]tetrahydro-3-furanyl benzoate

생성물 1

HCID 10305241(2S,3S,4R,5R)-5-(6-[(2,2-Diphenylethyl)amino]-2-{[({[2-(1-piperidinyl)ethyl]amino}carbonyl)amino]methyl}-9H-purin-9-yl)-N-ethyl-3,4-dihydroxytetrahydro-2-furancarboxamide
수율 19.5%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Potassium carbonate (20 mg, 0.14 mmol) was added to a solution of (2S,3S,4R,5R)-4-(benzoyloxy)-5-(6-[(2,2-diphenylethyl)amino]-2-{[({[2-(1-piperidinyl)ethyl]amino}carbonyl)amino]methyl}-9H-purin-9-yl)-2-[(ethylamino)carbonyl]tetrahydro-3-furanyl benzoate (100 mg, 0.13 mmol) (Preparation 14) in methanol (100 ml). The reaction mixture was stirred at room temperature for 2 hours. More potassium carbonate (20 mg, 0.14 mmol) was then added and the reaction mixture was heated to 60° C. for 2 hours. The solvent was removed under reduced pressure to give a residue that was slurried with acetone and filtered. The filtrate was evaporated under reduced pressure and the residue was partially purified by column chromatography on silica gel eluting with dichloromethane:methanol:0.88 concentrated aqueous ammonia (90:10:1 by volume). The residue after solvent evaporation under reduced pressure was repurified by more column chromatography on silica gel eluting with dichloromethane:methanol:0.88 concentrated aqueous ammonia (90:10:1 by volume). The solvent was removed by evaporation under reduced pressure to give the title compound as a foam (17 mg).

후처리

  1. temperaturethe reaction mixture was heated to 60° C. for 2 hours
  2. customThe solvent was removed under reduced pressure
  3. customto give a residue that
  4. filtrationfiltered
  5. customThe filtrate was evaporated under reduced pressure
  6. customthe residue was partially purified by column chromatography on silica gel eluting with dichloromethane
  7. customThe residue after solvent evaporation under reduced pressure
  8. customwas repurified by more column chromatography on silica gel eluting with dichloromethane
  9. customThe solvent was removed by evaporation under reduced pressure

출처 및 근거

ORD 기록
ord-9f74dbb77ee84360b5cce84545194b90
출처 데이터셋
uspto-grants-2005_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06921753B2

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