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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976945Generated: October 30, 2026

Triethylamine → Deoxyuridine Triphosphate

https://huagongshe.com/reaction/1976945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-(3-Amino)allyldeoxyuridine 5'-triphosphateHCID 86599380—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductDeoxyuridine TriphosphateHCID 65070—

Reaction Steps

To a solution of 2 mg of 5-(3-aminoallyl)-2′-deoxyuridine-5′-triphosphate, ammonium salt (Sigma Chemical) in 100 μL of water is added a solution of 3 mg of Compound 72 (Example 73) in 100 μL of DMF, followed by addition of 5 μL of triethylamine. After the mixture is stirred at room temperature for 3 hours, the solution is evaporated to dryness under vacuum and the residue is purified by chromatography over lipophilic SEPHADEX resin using water for elution. The first green fluorescent fractions are combined and lyophilized to give the fluorescent nucleotide conjugate as an orange solid (Compound 107) Alternatively a fluorescent conjugate (Compound 108) of deoxyuridine-5′-triphosphate is prepared using 5-(3-amino-1-propynyl)-2′-deoxyuridine-5′-triphosphate in place of 5-(3-aminoally)-2′-deoxyuridine-5′-triphosphate (as described in Hobbs, Jr. et al, supra).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06229055B1
Source datasetuspto-grants-2001_05
ORD IDord-34546c0d15c847888c723c0442c97165
Source noteuspto-grants-2001_05