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
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulphonyl cyanide | HCID 87946 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 6-Ethynylisoquinoline | HCID 57950541 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(Isoquinolin-6-yl)propiolonitrile | HCID 57950667 | 56% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897619B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-245ca8ef74164bcc8a57141d485ba1d4 |
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| Source note | uspto-grants-2011_03 |
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