化工社化工社 化学情報印刷レポート · 研究参考用
Formaldehyde → 1,2,3,9-Tetrahydro-9-methyl-3-methylene-4H-carbazol-4-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Formaldehyde | HCID 712 | — |
| 反応物 | Ondansetron | HCID 4595 | — |
| 反応物 | Morpholine | HCID 8083 | — |
| 反応物 | 9-Methyl-1,2,3,9-tetrahydro-4H-carbazol-4-one | HCID 598875 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 1,2,3,9-Tetrahydro-9-methyl-3-methylene-4H-carbazol-4-one | HCID 11790505 | — |
反応手順
Kim et al. (Heterocycles 1997, 45, 2041) disclose a two-step synthesis of ondansetron. In the first step of the synthesis, 1,2,3,9-tetrahydro-9-methyl-4H-carbazol-4-one (compound of formula 1, Scheme 1) is reacted with a source of formaldehyde and morpholine in boiling glacial acetic acid to provide 1,2,3,9-tetrahydro-9-methyl-3-methylene-4H-carbazol-4-one (compound of formula 2, Scheme 1). In the second step of the synthesis, 1,2,3,9-tetrahydro-9-methyl-3-methylene-4H-carbazol-4-one is reacted with 2-methylimidazole in the presence of alumina (Al2O3) to provide ondansetron (See, Scheme 1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07696356B2 |
| 出典データセット | uspto-grants-2010_04 |
| ORD ID | ord-ab14a4ed59114cde9f6a7f164b3efe91 |
| 出典メモ | uspto-grants-2010_04 |