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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511589Generated: October 28, 2026

Triphenylphosphine → HCID 86300601, compound

https://huagongshe.com/reaction/511589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantDiphenylphosphoryl azideHCID 123414—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 67776590HCID 67776590—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86300601HCID 8630060183.4%

Reaction Steps

A solution of ((3aR,4R,6R,6aR)-6-(4-((2,4-dimethoxybenzyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol (2.83 g, 6.20 mmol) and triphenylphosphine (2.28 g, 8.68 mmol) in dry tetrahydrofuran (32 mL) was cooled at 0° C. in an ice/water bath. Diisopropyl azodicarboxylate (1.71 mL, 8.68 mmol) was added dropwise, followed by a solution of diphenylphosphonic azide (1.87 mL, 8.68 mmol) in tetrahydrofuran (5.3 mL, 66 mmol). Upon addition of the DPPA solution, a white milky precipitate formed. After about 30 minutes, the reaction mixture was allowed to warm to room temperature and stir overnight. After 24 h, HPLC indicated that all the starting material had been consumed. The reaction mixture was concentrated to about ½ the original volume and purified by flash chromatography (175 g silica gel, 10-55% EA/hept) to yield the title compound (2.49 g, 83%) as a slightly yellow stiff foam: MS (ESI+) for C23H27N7O5 m/z 482.2 (M+H)+; (ESI−) for C23H27N7O5 m/z 480.1 (M+H)−, m/z 526.1 (M+CO2H)−; HPLC purity 97%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096634B2
Source datasetuspto-grants-2015_08
ORD IDord-846036d4689b4ad0922b2617f1783715
Source noteuspto-grants-2015_08