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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707294Generated: October 29, 2026

Triphenylphosphine → HCID 178481627, compound

https://huagongshe.com/reaction/707294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant1-Methyl-1h-imidazo[4,5-b]pyridin-2(3h)-oneHCID 854236—
ReactantHCID 178454126HCID 178454126—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
ProductHCID 178481627HCID 178481627—

Reaction Steps

1-Methyl-1H-imidazo[4,5-b]pyridin-2(3H)-one (9.63 g, 64.6 mmol), tert-butyl(trans-3-hydroxycyclobutyl)carbamate (Intermediate 69, 12.1 g, 64.6 mmol), and triphenylphosphine (25.4 g, 97 mmol) were mixed in THF (250 mL) under an argon atmosphere at 0° C. Diisopropyl azodicarboxylate (19.0 mL, 97 mmol) was added dropwise via syringe, and the reaction mixture was warmed to room temperature and stirred for 18 h. The reaction mixture was diluted with saturated NaHCO3 and extracted with EtOAc (3×). The organic layer was separated, washed with brine, dried over MgSO4, filtered, and concentrated. The resulting crude product was purified via silica gel flash column chromatography eluting with 0 to 100% EtOAc in hexanes to yield the title compound as a yellow solid and used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174992B2
Source datasetuspto-grants-2015_11
ORD IDord-9888337a74364b0e8e90bbb38fd9efe2
Source noteuspto-grants-2015_11