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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethyl Phosphate | HCID 6535 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2-(6-Cyano-1-hexyn-1-yl)adenosine | HCID 11210971 | — |
| Product | Triethylammonium 2-(6-cyano-1-hexyn-1-yl)adenosine 5'-monophosphate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132409B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-7426ee97c9854d988c63cb17f13d2e4b |
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| Source note | uspto-grants-2006_11 |
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