HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromoaniline → 8-(3-Bromo-phenylamino)imidazo[4,5-g]quinoline-7-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | 8-Chloroimidazo[4,5-g]quinoline-7-carbonitrile | HCID 69372843 | — |
| Solvent | Glycol monoethyl ether | HCID 8076 | — |
| Product | 8-(3-Bromo-phenylamino)imidazo[4,5-g]quinoline-7-carbonitrile | HCID 69373246 | 63.1% |
Reaction Steps
A mixture of 0.2 g (0.87 mmol) of 8-chloroimidazo[4,5-g]quinoline-7-carbonitrile, 0.12 mL (1.1 mmol) of 3-bromoaniline, and 0.1 g (0.87 mmol) of pyridine hydrochloride in 5.0 mL of 2-ethoxyethanol is heated at reflux temperature for 45 minutes, then cooled to room temperature. The product mixture is poured into a saturated solution of sodium bicarbonate and stirred for 0.5 hour. The solid is collected by filtration, washed with water and dried. The solid is purified by silica gel chromatography, utilizing a gradient of methylene chloride/methanol(98:2 to 93:7) to yield 0.20 g of 8-(3-bromo-phenylamino)imidazo[4,5-g]quinoline-7-carbonitrile as pink solid, mp 286-288° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06638929B2 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-32fedfaad3874e4e8a9f552f112807f7 |
| Source note | uspto-grants-2003_10 |