Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105677Generated: November 1, 2026

Triphenylphosphine → HCID 18767693, compound

https://huagongshe.com/reaction/2105677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantAzidotrimethylsilaneHCID 78378—
ReactantDiethyl azodicarboxylateHCID 5462977—
ReactantHCID 18767616HCID 18767616—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18767693HCID 187676933.8%

Reaction Steps

A solution of N-(2-cyano-ethyl)-3-[4-(2,6-dioxo-1,3-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)-bicyclo[2.2.2]oct-1-yl]-propionamide (500 ng, 1.06 mmol, 1.0 eq), Ph3P (2.0 eq, 2.13 mmol, 560 mg), TMSN3 (2.0 eq, 2.13 mmol, 245 mg), and DEAD (2.0 eq, 2.13 mmol, 371 mg) in THF (10 ml) was stirred at rt for 24 h. The reaction vessel was re-charged with the reagent cocktail (2.0 eq, 2.13 mmol) and stirring was continued for an additional 24 h. The reaction was quenched by the addition of a 50% aqueous solution of (NH4)2Ce(NO3)6 and extracted with EtOAc. The combined organic extracts were washed with brine, dried over MgSO4, filtered and evaporated in vacuo to afford a viscous orange oil. A portion of the material was purified by preparative LC to afford 20 mg of pure material. MS: 494 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579354B2
Source datasetuspto-grants-2009_08
ORD IDord-475d56c461c64571b6f0c58f8e6972b8
Source noteuspto-grants-2009_08