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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5336Generated: October 23, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantN-tert-butyloxycarbonyl-L-norleucyl-proline amideHCID 53782269—
ProductL-norleucyl-L-proline amide hydrochlorideHCID 70082665—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244884
Source datasetuspto-grants-1993_09
ORD IDord-da46530a89434c3c8d249230d0da1142
Source noteuspto-grants-1993_09