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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172608Generated: October 27, 2026

2-(6-Bromoquinolin-4-yl)-1-(6-methylpyridin-2-yl)ethanone → 1-[2-(6-Bromo-quinolin-4-yl)-1-(6-methyl-pyridin-2-yl)-ethylideneamino]-pyrrolidin-2-one

https://huagongshe.com/reaction/1172608

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(6-Bromoquinolin-4-yl)-1-(6-methylpyridin-2-yl)ethanoneHCID 17980602—
Reactant1-Aminopyrrolidin-2-one hydrochlorideHCID 21992845—
SolventPyridineHCID 1049—
Product1-[2-(6-Bromo-quinolin-4-yl)-1-(6-methyl-pyridin-2-yl)-ethylideneamino]-pyrrolidin-2-oneHCID 5895882669.7%

Reaction Steps

Stir a mixture of 2-(6-bromo-quinolin-4-yl)-1-(6-methyl-pyridin-2-yl)-ethanone (38.5 g, 113 mmol) and 1-aminopyrrolidinone hydrochloride (20 g, 147 mmol) in 115 mL pyridine at ambient temperature for 10 hours. Add about 50 g of 4 Å unactivated sieves. Continue stirring an additional 13 h and add 10-15 g silica and filter the mixture through a 50 g silica plug. Elute the silica plug with 3 L ethyl acetate. Combine the filtrates and concentrate in vacuo. Collect the hydrazone precipitate by filtration and suction dry to yield 33.3 g (69.7%) of the desired subtitled intermediate as an off-white solid. MS ES+=423 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834029B2
Source datasetuspto-grants-2010_11
ORD IDord-b2b9c31bb00d4111b526e977283d96f0
Source noteuspto-grants-2010_11