HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018820Generated: October 26, 2026
Water → 2'-(N-Lysyl)amino-2'-deoxy-cytidine Triphosphate
https://huagongshe.com/reaction/1018820
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Pyrophosphate | HCID 644102 | — |
| Reactant | Triphosphate | HCID 3440921 | — |
| Reactant | Tributyl ammonium pyrophosphate | HCID 21910867 | — |
| Reactant | 2'-(N-lysyl)amino 2'-deoxy cytidine | HCID 22899181 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Triethyl Phosphate | HCID 6535 | — |
| Product | 2'-(N-Lysyl)amino-2'-deoxy-cytidine Triphosphate | HCID 22899186 | — |
Reaction Steps
2′-(N-lysyl)amino 2′-deoxy cytidine (0.180 g, 0.22 mmol) was dissolved in triethyl phosphate (2.00 ml) under Ar. The solution was cooled to 0° C. in an ice bath. Phosphorus oxychloride (99.999%, 3 eq., 0.0672 mL) was added to the solution and the reaction was stirred for two hours at 0° C. Tributylammonium pyrophosphate (4 eq., 0.400 g) was dissolved in 3.42 mL of acetonitrile and tribuytylamine (0.165 mL). Acetonitrile (1 mL) was added to the monophosphate solution followed by the pyrophosphate solution which was added dropwise. The solution was clear. The reaction was allowed to warm up to room temperature. After stirring for 45 minutes, methyl amine (5 mL) was added and the reaction and stirred at room temperature for 2 hours. A two phase mixture appeared (little beads at the bottom of the flask). TLC (7:1:2 iPrOH:NH4OH:H2O) showed the appearance of a triphosphate material. The solution was concentrated, dissolved in water and loaded on a newly prepared DEAE Sephadex A-25 column. The column was washed with a gradiant up to 0.6 M TEAB buffer and the product eluted off in fractions 90-95. The fractions were analyzed by ion exchange HPLC. Each fraction showed one triphosphate peak that eluted at ˜4.000 minutes. The fractions were combined and pumped down from methanol to remove buffer salt to yield 15.7 mgs of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06482932B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-b00396d83aa6400e9dba41e38b97947e |
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| Source note | uspto-grants-2002_11 |
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