HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920691Generated: October 30, 2026
2'-Deoxy-2'-fluoro-2'-methyluridine → HCID 45102209, compound
https://huagongshe.com/reaction/1920691
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2'-Deoxy-2'-fluoro-2'-methyluridine | HCID 11311503 | — |
| Reactant | HCID 131729699 | HCID 131729699 | — |
| Reactant | HCID 178418441 | HCID 178418441 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 45102209 | HCID 45102209 | — |
Reaction Steps
To a stirred solution of 1-((2R,3R,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione (730 mg, 2.8 mmol) in dry pyridine (15 mL) was added a 0.45M solution of tetrazole in acetonitrile (15 mL) followed by bis(N,N-diisopropylamino)methylphosphite (0.971 mL, 3.3 mmol) at room temperature. After 2 h, TLC indicated disappearance of the starting material and two non-polar products. The reaction mixture was concentrated under reduced pressure at room temperature and the residue was triturated with EtOAc (30 mL). Tetrazole salts precipitated were filtered off and the filtrate was concentrated under reduced pressure. The residue was chromatographed using 0-40% EtOAc/hexanes gradient to give pure product 2 (92 mg) and mixture of product 1&2 (102 mg). 1H NMR confirmed that the product 2 is a single isomer of the required compound. Stereochemistry is not determined.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173621B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-a11a138ffd5445958ccbda82a7eeb51c |
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| Source note | uspto-grants-2012_05 |
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