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Sodium Hydroxide → 9-((2R,3S,4R,5R)-3,4-Bis(benzyloxy)-5-((benzyloxy)methyl)tetrahydrofuran-2-yl)-2-fluoro-9H-purin-6-amine

HRID 1448996
ノート
印刷プレビュー

反応式

HRID 1448996 の反応式
[H+].[B-](F)(F)(F)[F:3].N[C:8]1[N:16]=[C:15]2[C:11]([N:12]=[CH:13][N:14]2[C@@H:17]2[O:37][C@H:36]([CH2:38][O:39][CH2:40][C:41]3[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=3)[C@@H:27]([O:28][CH2:29][C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)[C@@H:18]2[O:19][CH2:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[C:10]([NH2:47])[N:9]=1.[OH-].[Na+]>C(Cl)(Cl)Cl.O>[CH2:20]([O:19][C@H:18]1[C@H:27]([O:28][CH2:29][C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)[C@@H:36]([CH2:38][O:39][CH2:40][C:41]2[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=2)[O:37][C@H:17]1[N:14]1[CH:13]=[N:12][C:11]2[C:15]1=[N:16][C:8]([F:3])=[N:9][C:10]=2[NH2:47])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 14798Sodium HydroxideHCID 28118Tetrafluoroboric acidHCID 108969412-Amino-9-(2,3,5-tri-O-benzyl-beta-D-arabinofuranosyl)adenine

生成物 1

HCID 109627089-((2R,3S,4R,5R)-3,4-Bis(benzyloxy)-5-((benzyloxy)methyl)tetrahydrofuran-2-yl)-2-fluoro-9H-purin-6-amine

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6212
Chloroform
溶媒
2 回

実験手順

HBF4 (48%) (150 ml) was added to a solution (5°) of 2-amino-9-(2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)adenine (III, 4.6 g, 8.4 mmol) in CHCl3 (60 ml). The resulting mixture was cooled to -10° before a solution of N--NO2 (17 g, 25 mmol) in 4 ml of H2O was added dropwise with stirring. After the addition was complete, the mixture was stirred an additional 40 min. at -10° to -5° before it was diluted with CHCl3 (75 ml), cooled to -20°, and neutralized (pH 5-6) with 50% NaOH. The CHCl3 layer was separated, washed with H2O, dried (MgSO4), and evaporated to dryness in vacuo. The residue, primarily a mixture of II and 9-(2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)-2,6-difluoropurine, identified by TLC (1:1 CHCl3 -EtOAc), was dissolved in absolute EtOH, and the solution was saturated at 5° with dry NH3. After refrigeration overnight, the reaction solution was evaporated to dryness in vacuo. The residue was dissolved in CHCl3 (25 ml), and the solution was filtered through dry Celite to remove inorganic salts. The filtrate was adsorbed on a silica gel column (2.6×35 cm, packed and equilibrated with CHCl3). The column was eluted with 1:1 CHCl3 -EtOAc. The fractions containing II were combined and evaporated to dryness in vacuo, and the residue was recrystallized from C6H6 (40 ml); yield 1.7 g (36%); mp 157°-159°; λmax (mμ), pH 1, 7, 13, and EtOH--261, 272 (sh); vmax (cm-1) 3350, 3320, 3150 (NH), 2940, 2920, 2910, 2860 (CH), 1665, 1610, 1575 (NH, C=C, C=N), 1110, 1100, 1085, 1060 (COC), 730 (phenyl).

後処理

  1. additionwas added dropwise
  2. additionAfter the addition
  3. stirringthe mixture was stirred an additional 40 min. at -10° to -5° before it
  4. temperaturecooled to -20°
  5. customThe CHCl3 layer was separated
  6. washwashed with H2O
  7. dry with materialdried (MgSO4)
  8. customevaporated to dryness in vacuo
  9. additionThe residue, primarily a mixture of II and 9-(2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)-2,6-difluoropurine
  10. dissolutionwas dissolved in absolute EtOH
  11. customwas saturated at 5° with dry NH3
  12. customthe reaction solution was evaporated to dryness in vacuo
  13. dissolutionThe residue was dissolved in CHCl3 (25 ml)
  14. filtrationthe solution was filtered
  15. customthrough dry Celite
  16. customto remove inorganic salts
  17. washThe column was eluted with 1:1 CHCl3 -EtOAc
  18. additionThe fractions containing II
  19. customevaporated to dryness in vacuo
  20. customthe residue was recrystallized from C6H6 (40 ml)

出典と根拠

ORDレコード
ord-ec473e4b54b24c5dab27491673679f55
出典データセット
uspto-grants-1980_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04188378

反応ノート

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