HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(6-Bromoquinolin-4-yl)-1-(6-methylpyridin-2-yl)ethanone | HCID 17980602 | — |
| Reactant | 1-Aminopyrrolidin-2-one hydrochloride | HCID 21992845 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 1-[2-(6-Bromo-quinolin-4-yl)-1-(6-methyl-pyridin-2-yl)-ethylideneamino]-pyrrolidin-2-one | HCID 58958826 | 69.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07834029B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-b2b9c31bb00d4111b526e977283d96f0 |
| Source note | uspto-grants-2010_11 |