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Water → 3'-Azido-2',3'-dideoxyuridine 5'-monophosphate

HRID 467264
ノート
印刷プレビュー

反応式

HRID 467264 の反応式
C(CC[O:5][P:6]([O-])([O-:8])=[O:7])#N.[N:10]([C@@H:13]1[C@@H:17]([CH2:18][OH:19])[O:16][C@@H:15]([N:20]2[CH:27]=[CH:26][C:24](=[O:25])[NH:23][C:21]2=[O:22])[CH2:14]1)=[N+:11]=[N-:12].C1(N=C=NC2CCCCC2)CCCCC1.O>N1C=CC=CC=1.[OH-].[K+]>[P:6]([O:19][CH2:18][C@H:17]1[O:16][C@@H:15]([N:20]2[CH:27]=[CH:26][C:24](=[O:25])[NH:23][C:21]2=[O:22])[CH2:14][C@@H:13]1[N:10]=[N+:11]=[N-:12])([OH:8])([OH:7])=[O:5]
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 4

HCID 962WaterHCID 10868DicyclohexylcarbodiimideHCID 55262NavuridineHCID 4064087beta-Cyanoethyl phosphate

生成物 1

HCID 1594863'-Azido-2',3'-dideoxyuridine 5'-monophosphate収率 73%

試薬・触媒・溶媒 2

HCID 1049Pyridine
溶媒
2 回
HCID 14797Potassium Hydroxide溶媒

実験手順

A freshly prepared pyridinium salt of 2-cyanoethylphosphate (8.05 g, 23.64 mmol) was added to a solution of 3'-azido-2',3'-dideoxyuridine (2.50 g, 9.7 mmol) in dry pyridine (50 ml) and evaporated to dryness at 30° C. The concentrated residue was dissolved in pyridine (50 ml) and the solution again evaporated to dryness. The process was repeated twice and then the residue obtained was dissolved in dry pyridine (50 ml). Dicyclohexylcarbodiimide (8.08 g, 39.1 mmol) was added to the solution. The reaction mixture was stirred for 48 hours at room temperature. Water (10 ml) was added and the solution was then filtered to remove dicyclohexylurea. The clear solution was evaporated to dryness. The residue obtained was then dissolved in 1N KOH (250 ml) and heated for 15 minutes at 100° C. The cold solution was passed through a column of acidic Dowex 50 (H+), the effluent brought to pH 9 and passed through a column of Dowex (1×4 Cl-). A linear gradient elution of 0.015N HCl to 0.15N HCl resulted in 3'-azido-2',3'-dideoxyuridine-5'-monophosphate with a 73% yield.

後処理

  1. customevaporated to dryness at 30° C
  2. dissolutionThe concentrated residue was dissolved in pyridine (50 ml)
  3. customthe solution again evaporated to dryness
  4. customthe residue obtained
  5. filtrationthe solution was then filtered
  6. customto remove dicyclohexylurea
  7. customThe clear solution was evaporated to dryness
  8. customThe residue obtained
  9. temperatureheated for 15 minutes at 100° C
  10. washA linear gradient elution of 0.015N HCl to 0.15N HCl
  11. customresulted in 3'-azido-2',3'-dideoxyuridine-5'-monophosphate with a 73% yield

出典と根拠

ORDレコード
ord-68ca896be8d043ec87e3ddc71e971c91
出典データセット
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05159067

反応ノート

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