Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598835Generated: October 31, 2026

Acetonitrile → 3-(Isoquinolin-6-yl)-3-oxopropanenitrile

https://huagongshe.com/reaction/598835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant6-Isoquinolinecarboxylic acid, methyl esterHCID 15290360—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Product3-(Isoquinolin-6-yl)-3-oxopropanenitrileHCID 57950568100%

Reaction Steps

To a solution of ACN (1.8 g, 43 mmol) in 90 mL of THF at −78° C. was added tert-butyllithium (25 mL, 1.7 M in heptane). After 20 minutes, methyl isoquinoline-6-carboxylate (2.0 g, 11 mmol) was added slowly in 10 mL of THF. After 1 hour, the reaction was quenched with 100 mL of aqueous NH4Cl and warmed to room temperature. The biphasic mixture was extracted twice with 100 mL of EtOAc, and the combined organic extracts were washed with 100 mL of brine and dried over MgSO4. Filtration and concentration under reduced pressure afforded 3-(isoquinolin-6-yl)-3-oxopropanenitrile (2.1 g, 100% yield crude). The product thus obtained was used in the next step without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897619B2
Source datasetuspto-grants-2011_03
ORD IDord-226bf91ae26b4e42a0520fc7d03d62e4
Source noteuspto-grants-2011_03