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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252711Generated: November 3, 2026

Triphenylphosphine → HCID 3011897, compound

https://huagongshe.com/reaction/2252711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant4-Chloro-5-fluoro-7H-pyrrolo(2,3-d)pyrimidineHCID 11321224—
Reactant2,3,5-Tri-O-benzoyl-2-C-methyl-D-ribofuranoseHCID 57376970—
SolventTetrahydrofuranHCID 8028—
ProductHCID 3011897HCID 3011897—

Reaction Steps

To a solution of the compound from Step C (0.075 g, 0.44 mmol), 2,3,5-tri-O-benzoyl-2-C-methyl-D-ribofuranose [Harry-O'kuru, Rogers E.; Smith, Jennifer M.; Wolfe, Michael S, “A Short, Flexible Route toward 2′-C-Branched Ribonucleosides,” J. Org. Chem., 62: 1754-1759 (1997)] (4-5) (0.25 g, 0.53 mmol) and triphenylphosphine (0.23 g, 0.88 mmol) in THF (15 mL) was added diethyl azodicarboxylate (DEAD) (0.14 mL, 0.88 mmol). The reaction mixture was stirred at room temperature overnight. The solution was directly adsorbed onto silica gel and purified over silica gel using ethyl acetate/hexane 1:9 as the eluent Appropriate fractions were dissolved in dioxane (3 mL) and liquid ammonia (4 mL) and the mixture was heated in a steel bomb at 85° C. for 24 h. The solvent was evaporated and the residue was purified over silica gel using methanol/dichloromethane (1:9) as the eluent. Fractions containing the desired compound were pooled and evaporated in vacuo to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323453B2
Source datasetuspto-grants-2008_01
ORD IDord-4e5d69bbec084ad8a5c87d62bb126d20
Source noteuspto-grants-2008_01