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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097634Generated: October 25, 2026

Triphenylphosphine → HCID 59395803, compound

https://huagongshe.com/reaction/1097634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1,2-Bis(phenylmethyl) 1,2-diazenedicarboxylateHCID 75557—
Reactant3-(1H-pyrazol-4-yl)propan-1-olHCID 3578384—
Reactant7-Allyl-8-chloro-3-pentyl-1H-purine-2,6(3H,7H)-dioneHCID 59299557—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59395803HCID 5939580342.5%

Reaction Steps

3-Pentyl-8-chloro-7-(2-propen-1-yl)-3,7-dihydro-1H-purine-2,6-dione (5 g, 16.86 mmol) and 3-(1H-pyrazol-4-yl)propan-1-ol (2.12 g, 16.8 mmol) were stirred in dry THF (150 ml) at 3° C. Dibenzyl azodicarboxylate (10.05 g, 33.7 mmol) was added followed by the dropwise addition of triphenylphosphine (8.83 g, 33.7 mmol) in dry THF (70 ml). The mixture was allowed to warm to it and stirred for 18 h. Water (1 ml) was added and the solvents evaporated. The residue was taken up in Et2O (200 ml) from which a white solid, mostly triphenylphosphine oxide, crystallised and was filtered off. The filtrate was concentrated and further by-products crystallised from ether-cyclohexane. The remaining filtrate was concentrated (19.2 g) and purified on a Biotage™ system (400 g) eluting with EtOAc-cyclohexane (2:1) to afford the title compound as a white solid (2.89 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143264B2
Source datasetuspto-grants-2012_03
ORD IDord-a351c52f866a4ef3827555a2cc86e10d
Source noteuspto-grants-2012_03