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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethylamineHCID 6329—
ReactantAmmonium HydroxideHCID 14923—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantPyrophosphateHCID 644102—
ReactantTriphosphateHCID 3440921—
ReactantTributyl ammonium pyrophosphateHCID 21910867—
Reactant2'-(N-lysyl)amino 2'-deoxy cytidineHCID 22899181—
SolventIsopropanolHCID 3776—
SolventAcetonitrileHCID 6342—
SolventTriethyl PhosphateHCID 6535—
Product2'-(N-Lysyl)amino-2'-deoxy-cytidine TriphosphateHCID 22899186—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06482932B1
Source datasetuspto-grants-2002_11
ORD IDord-b00396d83aa6400e9dba41e38b97947e
Source noteuspto-grants-2002_11