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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598841Generated: October 31, 2026

p-Toluenesulphonyl cyanide → 3-(Isoquinolin-6-yl)propiolonitrile

https://huagongshe.com/reaction/598841

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulphonyl cyanideHCID 87946—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant6-EthynylisoquinolineHCID 57950541—
SolventTetrahydrofuranHCID 8028—
Product3-(Isoquinolin-6-yl)propiolonitrileHCID 5795066756%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 6-ethynylisoquinoline (0.10 g, 0.65 mmol) in 6.5 mL of THF at −78° C. was added LiHMDS, (0.78 mL, 1.0 M in THF). After 5 minutes, the mixture was warmed to 0° C. The mixture was stirred for 30 minutes and then chilled to −78° C. Tosyl cyanide (0.18 g, 0.98 mmol) was added. After 5 minutes, the reaction was warmed to 0° C. and stirred for 1 hour. The reaction was quenched with 10 mL of aq. NH4Cl. The biphasic mixture was extracted twice with 10 mL of EtOAc and the combined organic extracts were washed with 15 mL of brine and dried over MgSO4. Filtration and concentration under reduced pressure, followed by flash chromatography on silica gel (5% to 20% EtOAc/hexanes) afforded 3-(isoquinolin-6-yl)propiolonitrile (0.065 g, 0.36 mmol, 56% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897619B2
Source datasetuspto-grants-2011_03
ORD IDord-245ca8ef74164bcc8a57141d485ba1d4
Source noteuspto-grants-2011_03