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Synthesis of the arginine labelled by {sup 15}N on the amidine group; Synthese de l'arginine marquee par {sup 15}N dans le groupe amidine

Abstract

For some biologic studies, it was necessarily to have (+) arginine marked by nitrogen 15 in the amidine group. This report describes the synthesis of the labelled arginine. The first step is the synthesis of the methyl-isourated hydro-chlorate, the intermediate reactive, from the ClNH{sub 4} isotope. The arginine is obtained from the ornithine which we previously blocked the amino group as cupric complex. The mean yield in arginine reaches 30%, based on the ammonium chloride uses. (M.B.) [French] Pour certaines etudes biologiques, il etait indispensable de disposer de (+) arginine marquee par l'azote 15 dans le groupement amidine. Ce rapport decrit la synthese de l'ariginine marquee. La premiere etape est la synthese du chlorhydrate de methylisouree, intermediaire reactif, a partir du ClNH{sub 4} isotopique. L'obtention de l'arginine est obtenue a partir de l'ornithine dont on a prealablement bloque le groupe amino sous forme de complexe cuivrique. Le rendement global moyen en arginine atteint 30 %, base sur le chlorure d'ammonium utilise. (M.B.)
Authors:
Pichat, L; Clement, J [1] 
  1. Commissariat a l'Energie Atomique, Saclay(France). Centre d'Etudes Nucleaires
Publication Date:
Jul 01, 1955
Product Type:
Technical Report
Report Number:
CEA-R-403
Resource Relation:
Other Information: 7 ref
Subject:
38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEAR CHEMISTRY; AMIDINES; ARGININE; CHEMICAL PREPARATION; CHEMICAL REACTION YIELD; LABELLED COMPOUNDS; LABELLING; NITROGEN 15; ORGANIC ION EXCHANGERS; ORNITHINE
OSTI ID:
20846041
Research Organizations:
CEA Saclay, 91 (France)
Country of Origin:
France
Language:
French
Other Identifying Numbers:
TRN: FR06R0403018202
Availability:
Available from INIS in electronic form
Submitting Site:
FRN
Size:
5 pages
Announcement Date:
Apr 02, 2007

Citation Formats

Pichat, L, and Clement, J. Synthesis of the arginine labelled by {sup 15}N on the amidine group; Synthese de l'arginine marquee par {sup 15}N dans le groupe amidine. France: N. p., 1955. Web.
Pichat, L, & Clement, J. Synthesis of the arginine labelled by {sup 15}N on the amidine group; Synthese de l'arginine marquee par {sup 15}N dans le groupe amidine. France.
Pichat, L, and Clement, J. 1955. "Synthesis of the arginine labelled by {sup 15}N on the amidine group; Synthese de l'arginine marquee par {sup 15}N dans le groupe amidine." France.
@misc{etde_20846041,
title = {Synthesis of the arginine labelled by {sup 15}N on the amidine group; Synthese de l'arginine marquee par {sup 15}N dans le groupe amidine}
author = {Pichat, L, and Clement, J}
abstractNote = {For some biologic studies, it was necessarily to have (+) arginine marked by nitrogen 15 in the amidine group. This report describes the synthesis of the labelled arginine. The first step is the synthesis of the methyl-isourated hydro-chlorate, the intermediate reactive, from the ClNH{sub 4} isotope. The arginine is obtained from the ornithine which we previously blocked the amino group as cupric complex. The mean yield in arginine reaches 30%, based on the ammonium chloride uses. (M.B.) [French] Pour certaines etudes biologiques, il etait indispensable de disposer de (+) arginine marquee par l'azote 15 dans le groupement amidine. Ce rapport decrit la synthese de l'ariginine marquee. La premiere etape est la synthese du chlorhydrate de methylisouree, intermediaire reactif, a partir du ClNH{sub 4} isotopique. L'obtention de l'arginine est obtenue a partir de l'ornithine dont on a prealablement bloque le groupe amino sous forme de complexe cuivrique. Le rendement global moyen en arginine atteint 30 %, base sur le chlorure d'ammonium utilise. (M.B.)}
place = {France}
year = {1955}
month = {Jul}
}