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Hydrochloric Acid → 1-[[2-(5-Bromo-3-indolyl)-1,1-dimethylethyl]amino]-3-(2-methylphenoxy)-2-propanol hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Indole, 3-(2-amino-2-methylpropyl)-5-bromo- | HCID 13259 | — |
| 反応物 | o-CRESYL GLYCIDYL ETHER | HCID 16640 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 1-[[2-(5-Bromo-3-indolyl)-1,1-dimethylethyl]amino]-3-(2-methylphenoxy)-2-propanol hydrochloride | HCID 12619653 | — |
反応手順
(2-Methylphenoxymethyl)oxirane, 4.1 g. (0.025 mole) and 6.65 g. (0.025 mole) of 5-bromo-α,α-dimethyl-1H-indol-3-yl-ethaneamine were mixed and heated at 140° for 1 hr. The mixture was then cooled and dissolved in 40 ml. of acetonitrile while still warm. The product was converted to the hydrochloride salt by treatment of the solution with 5 N ethanolic HCl. The solvent was removed by distillation and the residue dissolved in 30 ml. of acetonitrile. The product crystallized from this solution, yield 11.0 g., m.p. 197°-199°. This material was recrystallized from methanol/isopropanol, yield 8.0 g., m.p. 198.0°-200.0° dec. (corr.).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04234595 |
| 出典データセット | uspto-grants-1980_11 |
| ORD ID | ord-24faa05a5cf64903a1ba4521dbd3f790 |
| 出典メモ | uspto-grants-1980_11 |