Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504178Generated: October 30, 2026

Triphenylphosphine → HCID 66961316, compound

https://huagongshe.com/reaction/1504178

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 numberUS09212187B2
Source datasetuspto-grants-2015_12
ORD IDord-13dff2b11e504f34849c4b168edb4fd8
Source noteuspto-grants-2015_12