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4-Chloropyridine hydrochloride → 3-(4-Pyridinylamino)-1H-indole-2-carboxylic acid ethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Chloropyridine hydrochloride | HCID 81852 | — |
| 反応物 | Ethyl 3-amino-1H-indole-2-carboxylate | HCID 732887 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | 3-(4-Pyridinylamino)-1H-indole-2-carboxylic acid ethyl ester | HCID 10468920 | 60.7% |
反応手順
A solution ethyl 3-aminoindole-2-carboxylate (4.94 g, 24.2 mmole) and 4-chloropyridine hydrochloride (3.63 g, 24.2 mmole) in 70 mL of 1-methyl-2-pyrrolidinone was heated at 165° C. for 6 hours. The reaction mixture was then quenched into water and the aqueous phase was washed with ethyl acetate. After basification with a potassium carbonate solution, a solid was filtered, rinsed with water and ether and dried to give 4.13 g of a brown solid. A 2.2 g portion was recrystallized from methanol (charcoal treatment) to give 1.40 g of an off-white solid, mp: 248-250° C. (dec.)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06022880 |
| 出典データセット | uspto-grants-2000_02 |
| ORD ID | ord-a919875414314a15ba1580536db8fa7c |
| 出典メモ | uspto-grants-2000_02 |