HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
3-Bromoaniline → 4-(3-Bromophenylamino)benzo[4,5]furo[3,2-b]pyridine-3-carbonitrile
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 3-Bromoaniline | HCID 11562 | — |
| Edukt | 4-Chlorobenzo[4,5]furo[3,2-b]pyridine-3 carbonitrile | HCID 9899399 | — |
| Lösungsmittel | Glycol monoethyl ether | HCID 8076 | — |
| Produkt | 4-(3-Bromophenylamino)benzo[4,5]furo[3,2-b]pyridine-3-carbonitrile | HCID 10970521 | 63,4% |
Reaktionsschritte
A solution of 300 mg (1.30 mmol) of 4-chlorobenzo[4,5]furo[3,2-b]pyridine-3-carbonitrile and 0.160 mL (1.43 mmol) of 3-bromoaniline in 8 mL of 2-ethoxyethanol is heated at reflux temperature for 24 hours. The reaction mixture is partitioned between ethyl acetate and saturated sodium bicarbonate. The organic layer is washed with saturated sodium bicarbonate, followed by brine, then dried over sodium sulfate, filtered through a pad of diatomaceous earth and concentrated in vacuo. The resultant solid is collected by filtration to give 300 mg (42%) of a beige solid, mp 242-245° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06638929B2 |
| Quelldatensatz | uspto-grants-2003_10 |
| ORD ID | ord-b2e5a98a6c8941f1ac2fb5c20131ae6a |
| Quellennotiz | uspto-grants-2003_10 |