HCID 54479933, compound → HCID 453628, compound
Reaction equation
P([O:5][CH2:6][C@@:7]1([CH2:22][N:23]=[N+:24]=[N-:25])[O:11][C@@H:10]([N:12]2[CH:20]=[C:18]([CH3:19])[C:16](=[O:17])[NH:15][C:13]2=[O:14])[CH2:9][C@@H:8]1[OH:21])(O)(O)=O>O>[N:23]([CH2:22][C@:7]1([CH2:6][OH:5])[O:11][C@@H:10]([N:12]2[CH:20]=[C:18]([CH3:19])[C:16](=[O:17])[NH:15][C:13]2=[O:14])[CH2:9][C@@H:8]1[OH:21])=[N+:24]=[N-:25]Participants
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Sufficient water is added to 100 g of egg-yolk phospholipids to bring the total volume to 1 liter. The mixture is stirred with a homomixer. Then, the mixture is homogenized with an emulsifier under a pressure of 300 kg/cm2 for 30 minutes, whereby an aqueous phospholipid dispersion is obtained 4'-Azidomethylthymidine 5'-monophosphate (20 g) and sodium chloride (18 g) are dissolved in enough water to bring the total volume to 1 liter. The aqueous phospholipid dispersion (850 mL) and the 4'-azidomethylthymidine 5'-monophosphate solution (850 mL) are mixed. The aqueous dispersion thus obtained is filtered through a membrane filter (pore size 0.45 m in diameter). The filtrate is sterilized at 120° C. for 20 minutes and then allowed to stand at -20° C. for 20 hours in a freezer. The frozen dispersion thus obtained is thawed by allowing it to stand at room temperature. An aqueous suspension of 4'-azidomethylthymidine 5'-monophosphate entrapped in phospholipid spherules is thereby obtained.
Workup
- customThe aqueous dispersion thus obtained
- filtrationis filtered through a membrane
- filtrationfilter (pore size 0.45 m in diameter)
- waitto stand at -20° C. for 20 hours in a freezer
- customThe frozen dispersion thus obtained
- customto stand at room temperature
- customis thereby obtained
Sources & evidence
- ORD record
- ord-5012331bb5db402f8b417066bffcb3f1
- Source dataset
- uspto-grants-1993_03
- Patent number
- US05192749
Reaction notes
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