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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416129Generated: November 1, 2026

Water → HCID 70338952, compound

https://huagongshe.com/reaction/1416129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-BromooctaneHCID 8140—
ReactantSodium hydrideHCID 24758—
Reactant2-[1-Fluoro-3-(octyloxy)isoquinolin-7-yl]pyrimidin-5-olHCID 53861366—
SolventDimethylformamideHCID 6228—
ProductHCID 70338952HCID 7033895290%

Reaction Steps

10 mmol of 1-fluoro-7-(5-hydroxypyrimidin-2-yl)-3-octyloxyisoquinoline are dissolved in 50 ml of DMF, and 11 mmol of sodium hydride are added. After the mixture has been stirred for 30 minutes, 11 mmol of 1-octyl bromide are added dropwise, and the mixture is stirred at 60° C. for a further 140 minutes and poured into water. The mixture is extracted with dichloromethane, the combined organic phases are dried, the solvent is removed in vacuo, and the residue is chromatographed on silica gel, giving 9 mmol of 7-[5-(octyloxy)pyrimidin-2-yl]-1-fluoro-3-octyloxyisoquinoline. 1-Fluoro-7-(5-hydroxypyrimidin-2-yl)-3-alkyloxyisoquinolines can for example be reacted analogously to Example 3 with 2-fluoroalkyl sulfonates, 2,3-difluoroalkyl sulfonates, 3-alkyloxirane-2-methyl sulfonates, (ω-bromoalkyl)cyclopropanes or 1-bromodimethylsilanylalkanes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05911913
Source datasetuspto-grants-1999_06
ORD IDord-46d16d2f5c6342aca292e851278ebd91
Source noteuspto-grants-1999_06