HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → 4-(2,3-dihydro-1H-indol-6-ylamino)-6,7-diethoxy-quinoline-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Chloro-6,7-diethoxyquinoline-3-carbonitrile | HCID 10778872 | — |
| Reactant | 6-Aminoindoline dihydrochloride | HCID 24801896 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(2,3-dihydro-1H-indol-6-ylamino)-6,7-diethoxy-quinoline-3-carbonitrile | HCID 10156260 | 106.3% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A solution of 400 mg (1.44 mM) of 4-chloro-6,7-diethoxy-quinoline-3-carbonitrile and 258 mg (1.88 mM) of 6-Aminoindoline dihydrochloride salt in 10 ml of ethanol was refluxed for 3 hours. To the warm solution was added 1 ml of 1M sodium carbonate and the sample was heated for 5 minutes at 100° C., then poured into 300 ml of ice water. The solid was collected, washed with water followed by ether and dried under vacuum at 80° C. The solid was dissolved in 50/50 methanol/chloroform and dried onto silica gel and purified by chromatography using a gradient of 20% to 50% acetone in hexane to yield 496 mg of the title compound as a tan solid: mass spectrum (electrospray, m/e): M+H 375.1, mp=121-124° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06288082B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-f3312fe737f84c328ee1d344ea7fa217 |
| Source note | uspto-grants-2001_09 |