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

HRID 892421

反応式

HRID 892421 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

7

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 (50ml) 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 afforded 3'-azido-2',3'-dideoxyuridine-5'-monophosphate in 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

出典と根拠

ORDレコード
ord-eac5e203664e4ca58a3d99419adfe31c
出典データセット
uspto-grants-1992_06
特許番号
US05118672

関連ノート

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