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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836298Generated: November 3, 2026

2-(Benzhydrylideneamino)-3-quinolin-4-yl-butyronitrile → 2-Amino-3-quinolin-4-yl-butyronitrile

https://huagongshe.com/reaction/1836298

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Benzhydrylideneamino)-3-quinolin-4-yl-butyronitrileHCID 23499201—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
Product2-Amino-3-quinolin-4-yl-butyronitrileHCID 23499168102.5%

Reaction Steps

To 2-(Benzhydrylideneamino)-3-quinolin-4-yl-butyronitrile (3.0 g, 7.3 mmol) in 30 ml dioxane, 1N HCl (30 ml, 29.99 mmol, was added and the reaction mixture stirred at room temperature overnight. The solution was then concentrated under reduced pressure, partitioned between water (10 ml) and EtOAc (10 ml). The organic layer was dried over sodium sulfate, filtered and concentrated to give 1.58 g (88%) of the product which was used as such for the subsequent step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777426B2
Source datasetuspto-grants-2004_08
ORD IDord-596929d7cb1c4815aaf9c9c6c807ca4f
Source noteuspto-grants-2004_08