Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719086Generated: October 28, 2026

Triethyl Phosphate → Triethylammonium 2-(6-cyano-1-hexyn-1-yl)adenosine 5'-monophosphate

https://huagongshe.com/reaction/719086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl PhosphateHCID 6535—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-(6-Cyano-1-hexyn-1-yl)adenosineHCID 11210971—
ProductTriethylammonium 2-(6-cyano-1-hexyn-1-yl)adenosine 5'-monophosphateHCID 69595338—

Reaction Steps

Under argon, A 2-(6-cyano-1-hexyn-1-yl)adenosine (2.41 g) was dissolved in triethyl phosphate (15 mL), and, under ice-cooling conditions, phosphorous oxychloride (25.2 mL, 3.9 eq.) was added thereto, followed by stirring at the same temperature for 5 hours. The reaction mixture was added dropwise to a 10% sodium hydroxide solution (300 mL), and the resultant mixture was washed with ether. The aqueous layer was separated and water was removed under reduced pressure, and the residue was purified by C18 silica gel column chromatography (0.1M triethylammonium acetate buffer:acetonitrile=100:0 to 60:40). The thus-obtained fraction was concentrated, and the concentrate was subjected to C18 silica gel column chromatography (water:acetonitrile=100:0 to 60:40), to thereby remove the triethylammonium acetate buffer. The residue was freeze-dried, to thereby yield 1.14 g of the above-titled compound as a colorless amorphous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132409B2
Source datasetuspto-grants-2006_11
ORD IDord-7426ee97c9854d988c63cb17f13d2e4b
Source noteuspto-grants-2006_11