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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 1448997
ノート
印刷プレビュー

反応式

HRID 1448997 の反応式
N[C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[C@@H:11]2[O:31][C@H:30]([CH2:32][O:33][CH2:34][C:35]3[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=3)[C@@H:21]([O:22][CH2:23][C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[C@@H:12]2[O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[C:4]([NH2:41])[N:3]=1.[H+].[B-](F)(F)(F)[F:44].N([O-])=O.[Na+].NC1N=C2C(NC=N2)=C(N)N=1.[OH-].[Na+]>O1CCCC1>[CH2:14]([O:13][C@H:12]1[C@H:21]([O:22][CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[C@@H:30]([CH2:32][O:33][CH2:34][C:35]2[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=2)[O:31][C@H:11]1[N:8]1[CH:7]=[N:6][C:5]2[C:9]1=[N:10][C:2]([F:44])=[N:3][C:4]=2[NH2:41])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 14798Sodium HydroxideHCID 28118Tetrafluoroboric acid2 回HCID 309762,6-DiaminopurineHCID 108969412-Amino-9-(2,3,5-tri-O-benzyl-beta-D-arabinofuranosyl)adenineHCID 23668193Sodium Nitrite2 回

生成物 1

HCID 10962708
9-((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 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 2-amino-9-(2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)adenine (14.5 g, 26.2 mmol) in a mixture of 500 ml tetrahydrofuran and 1 l. of 48% fluoboric acid at -15° in a 4-l. beaker equipped with a mechanical stirrer was added dropwise in 20 min a saturated aqueous solution of NaNO2 (7.2 g, 105 mmol). The addition of NaNO2 (5.4 g, 78.6 mmol) was repeated three times after which none of the 2-aminoadenine remained (TLC). The fluoroboric acid was neutralized with 50% NaOH keeping the temperature between -40 and 0°. The solution was extracted four times with CHCl3 (300 ml, 250 ml, and two 200-ml portions). The CHCl3 extract was washed with saturated NaCl solution and then dried over MgSO4 before it was evaporated to dryness in vacuo. The residual oil was dissolved in a liter of ethanolic NH3 (saturated at 0° ), and the solution was allowed to stand for three days at 0° before it was evaporated to dryness. The residue was recrystallized from 100 ml EtOH; yield 4.7 g. Additional material was recovered from the filtrate by recrystallization and preparative TLC. The total yield was 5.8 g (40%).

後処理

  1. customat -15°
  2. custombeaker equipped with a mechanical stirrer
  3. customthe temperature between -40 and 0°
  4. extractionThe solution was extracted four times with CHCl3 (300 ml, 250 ml, and two 200-ml portions)
  5. extractionThe CHCl3 extract
  6. washwas washed with saturated NaCl solution
  7. dry with materialdried over MgSO4 before it
  8. customwas evaporated to dryness in vacuo
  9. dissolutionThe residual oil was dissolved in a liter of ethanolic NH3 (saturated at 0° )
  10. customwas evaporated to dryness
  11. customThe residue was recrystallized from 100 ml EtOH
  12. customAdditional material was recovered from the filtrate by recrystallization and preparative TLC

出典と根拠

ORDレコード
ord-0c622c255ebf454eaf3d72cfb5e37c36
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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