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t-butoxycarbonyl-N-(6-methoxy-6-oxohexyl)-L-phenylalaninamide → N-(6-methoxy-6-oxohexyl)-L-phenylalaninamide monohydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | t-butoxycarbonyl-N-(6-methoxy-6-oxohexyl)-L-phenylalaninamide | HCID 12799279 | — |
| 反応物 | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | N-(6-methoxy-6-oxohexyl)-L-phenylalaninamide monohydrochloride | HCID 70402980 | — |
反応手順
To a solution of the title compound of Example 2 (43.1 g, 0.11 mole) in 100 ml of dioxane was added 100 ml of 6M hydrogen chloride/dioxane. After about 30 min. the solution was concentrated in vacuo to dryness and the residue triturated thoroughly with diethyl ether. The solid was collected and washed well with diethyl ether, giving 34.7 g of the title compound, which was used in subsequent reactions without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04722922 |
| 出典データセット | uspto-grants-1988_02 |
| ORD ID | ord-dfc940d1027e4824b71c811ac0ae7fe4 |
| 出典メモ | uspto-grants-1988_02 |