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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707277Generated: October 29, 2026

Triphenylphosphine → HCID 178454106, compound

https://huagongshe.com/reaction/707277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant1-Cyclopropyl-1H-imidazo[4,5-b]pyridin-2(3H)-oneHCID 18334875—
ReactantHCID 178454125HCID 178454125—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178454106HCID 178454106—

Reaction Steps

To a solution of tert-butyl(cis-3-hydroxycyclobutyl)carbamate (Intermediate 71) (0.502 g, 2.68 mmol), triphenylphosphine (Sigma-Aldrich, 0.932 ml, 4.02 mmol), 1-cyclopropyl-1H-imidazo[4,5-b]pyridin-2(3H)-one (0.47 g, 2.68 mmol) in THF (10.73 ml) cooled to 0° C. was added diisopropyl azodicarboxylate (Sigma-Aldrich, 0.791 ml, 4.02 mmol) dropwise. The ice bath was removed after 1 h of stirring to allow the mixture to warm to room temperature. After an additional 3 h stirring, the reaction mixture was diluted with EtOAc and washed with saturated NaHCO3 solution. The organic layer was directly loaded onto a Biotage samplet. Purification (0-100% EtOAc/hexane) produced the title compound that solidified upon drying, which was advanced to next step directly without further purification. M+1: 345.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174992B2
Source datasetuspto-grants-2015_11
ORD IDord-790017886ffb45108575169cdc3c9257
Source noteuspto-grants-2015_11