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1,4-Dioxane hydrochloride → L-norleucyl-L-proline amide hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| 反応物 | N-tert-butyloxycarbonyl-L-norleucyl-proline amide | HCID 53782269 | — |
| 生成物 | L-norleucyl-L-proline amide hydrochloride | HCID 70082665 | — |
反応手順
The N-tert-butyloxycarbonyl-L-norleucyl-proline amide (1 g, 3.05 mmol) was placed in a round bottom flask to which freshly prepared 4N HCl/dioxane (25 ml) was added. The solution was stirred for 1 hour. Evaporation of solvent in vacuo and then crystallization of an oily residue from methanol/ethyl ether gave the title compound as a crystal-line product (0.76 g, 95%); oil, [α]D -17.7° (C=1; DMF); Rf 0.31 (1-butanol/acetic acid/water 4:1:1), Rf 0.42 (1 butanol/acetic acid/water, 4:1:5, upper phase).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05244884 |
| 出典データセット | uspto-grants-1993_09 |
| ORD ID | ord-da46530a89434c3c8d249230d0da1142 |
| 出典メモ | uspto-grants-1993_09 |