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HRID 5336作成日:2026年10月23日

1,4-Dioxane hydrochloride → L-norleucyl-L-proline amide hydrochloride

https://huagongshe.com/ja/reaction/5336

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-Dioxane hydrochlorideHCID 20443148—
反応物N-tert-butyloxycarbonyl-L-norleucyl-proline amideHCID 53782269—
生成物L-norleucyl-L-proline amide hydrochlorideHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05244884
出典データセットuspto-grants-1993_09
ORD IDord-da46530a89434c3c8d249230d0da1142
出典メモuspto-grants-1993_09