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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773297Generated: November 3, 2026

Triphenylphosphine → 9-(3-cyclopropyl-propoxy)-2-((S)-1-[1,4]dioxan-2-ylmethoxy)-6,7-dihydro-pyrimido[6,1-a]isoquinolin-4-one

https://huagongshe.com/reaction/1773297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4,4-Dimethyl-1-pentanolHCID 18393—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant(S)-2-((1,4-dioxan-2-yl)methoxy)-9-hydroxy-6,7-dihydro-4H-pyrimido[6,1-a]isoquinolin-4-oneHCID 136409086—
Solvent1,4-DioxaneHCID 31275—
Product9-(3-cyclopropyl-propoxy)-2-((S)-1-[1,4]dioxan-2-ylmethoxy)-6,7-dihydro-pyrimido[6,1-a]isoquinolin-4-oneHCID 86688461—

Reaction Steps

Intermediate 6 (2.12 g, 2.42 mmol, 1 eq.), 4,4-dimethyl-pentan-1-ol (0.77 g, 7.71 mmol, 1.2 eq.) and PPh3 (2.02 g, 7.71 mmol, 1.2 eq.) were suspended in 1,4-dioxane (50 mL) and the mixture was degassed with N2. DIAD (1.56 mL, 7.71 mmol, 1.1 eq.) was added dropwise and the reaction was stirred at RT for 2 h. The reaction mixture was quenched with brine and extracted with EtOAc, the organic phase was dried over MgSO4 and evaporated to dryness. Compound 143 was obtained by purification by flash chromatography on silica gel, eluting from 60 to 100% EtOAc/H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255095B2
Source datasetuspto-grants-2016_02
ORD IDord-e679162b4c9945d9aea37e0913b2ad19
Source noteuspto-grants-2016_02