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(4-Aminophenoxy)benzene → 4-(4-Phenoxyphenylamino)benzo[4,5]furo[3,2-b]pyridine-3-carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (4-Aminophenoxy)benzene | HCID 8764 | — |
| 反応物 | 4-Chlorobenzo[4,5]furo[3,2-b]pyridine-3 carbonitrile | HCID 9899399 | — |
| 溶媒 | Glycol monoethyl ether | HCID 8076 | — |
| 生成物 | 4-(4-Phenoxyphenylamino)benzo[4,5]furo[3,2-b]pyridine-3-carbonitrile | HCID 10270927 | 35% |
反応手順
A mixture of 200 mg (0.88 mmol) of 4-chlorobenzo[4,5]furo[3,2-b]pyridine-3-carbonitrile and 180 mg (0.96 mmol) of 4-phenoxyaniline in 5 mL of 2-ethoxyethanol is heated at reflux temperature for 3 hours. The reaction mixture is cooled to room temperature and 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 and filtered through a pad of diatomaceous earth. Concentration in vacuo yields 115 mg (35%) of a beige solid, mp 175-179° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06638929B2 |
| 出典データセット | uspto-grants-2003_10 |
| ORD ID | ord-bd042e1ef94342ad852d3fcc52e5e18c |
| 出典メモ | uspto-grants-2003_10 |