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4-Cyanobenzoyl chloride → Lecozotan
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Cyanobenzoyl chloride | HCID 80172 | — |
| 反応物 | {(R)-2-[4-(2,3-dihydrobenzo[1,4]dioxin-5-yl)piperazin-1-yl]propyl}-pyridin-2-ylamine | HCID 11279673 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Lecozotan | HCID 10116877 | — |
反応手順
A solution of {(R)-2-[4-(2,3-dihydrobenzo[1,4]dioxin-5-yl)piperazin-1-yl]propyl}-pyridin-2-ylamine (0.846 g, 2.38 mmol) in dichloromethane (20 mL) was treated at 0° C. with the dropwise addition of a dichloromethane solution of 4-cyanobenzoyl chloride (1.1 equivalents, 2.63 mmol in 5 mL). After stirring for 16 hours the mixture was poured onto hexane (100 mL) to precipitate the titled compound as its mono-hydrochloride salt (white solid, 1.2 g, 97% yield), which was recrystallized from dichloromethanelhexane.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07816362B2 |
| 出典データセット | uspto-grants-2010_10 |
| ORD ID | ord-e87ece455fc749de9fed5b3e9445e017 |
| 出典メモ | uspto-grants-2010_10 |