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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69007Generated: October 28, 2026

Triphenylphosphine → HCID 66961316, compound

https://huagongshe.com/reaction/69007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
Reactant6-hydroxyisoquinolin-1(2H)-oneHCID 10511170—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
Reactant3-[(2-Pyridin-3-ylethyl)pyridin-4-ylmethylamino]propan-1-olHCID 66960937—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 66961316HCID 66961316—

Reaction Steps

Triphenyl phosphine (51 mg) and di-tert-butyl azodicarboxylate (45 mg) were added to a tetrahydrofuran (THF) solution (1.5 ml) of 6-hydroxy-2H-isoquinolin-1-one (29 mg), and 3-[(2-pyridin-3-ylethyl)pyridin-4-ylmethylamino]propan-1-ol (40 mg). The mixture was stirred overnight. After the reaction mixture was condensed under reduced pressure, the residue was purified by NH silica gel column chromatography (ethyl acetate:methanol=1:0→4:1). The purified product was condensed under reduced pressure. A 4N-hydrogen chloride ethyl acetate solution (0.06 ml) was added to an ethyl acetate solution of the residue, which was stirred at room temperature for 30 minutes. The generated insoluble matter was separated by filtration, and was dried to produce the title compound (31.4 mg) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822453B2
Source datasetuspto-grants-2014_09
ORD IDord-c0ad8bb8176545f9b34b0cc3b92a29b2
Source noteuspto-grants-2014_09