The reaction o f amnonia-l5N w i t h benzaldehyde i n 50% aq. methanol followed by slow removal o f solve t l e d t o a high y i e l d o f a c r y s t a l l i n e product (benzylimine-r5N). On reduction with sodium cyanoborohydride a good y i e l d o f benzylamine-15N was obtained. The syntheti c u
A convenient synthesis of creatine-15N from glycine-15N via sarcosine-15N
β Scribed by W. Greenaway; F. R. Whatley
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- French
- Weight
- 184 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0022-2135
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β¦ Synopsis
The pre aration of creatine-' 5N monohydrate from intermediate is described.
15N) is converted to benzenesulphonyl glycine-I 5N, which is methylated to give benzenesulphonyl sarcosine--l5N. The latter is hydrolysed to sarcosine-l 5N1 which is isolated by ion exchange chromatography. Sarcosine-l5N is converted to creatine-l5N monohydrate by reaction with cyanamide in aqueous solution in the presence of sodium chloride and catalytic amounts of ammonium hydroxide-14N. The creatine-15N monohydrate precipitated from the above reaction mix is recrystallized from boiling water. The yield of sarcosine-15N from glycine-15N is 78% of theory and that of recrystallized creatine-15N monohydrate from glycine-15N is 59% of theory.
glycine-1 F N with the isolation of sarcosine-15N as an Glycine-15N (97.3 atom%
π SIMILAR VOLUMES
Condensation of guanidine-15N3 with 4-[ N( 2-amino-3-cyano-5-pyrazinylmethyl)-N-methylamino] benzoic acid (1) in refluxing methanol afforded 4amino-4-deoxy-N10-methylpteroic-3-15N-2-15NH2 (2). indicated no label introduction at the pterin N1 position. Coupling of 2. with diethyl L-gluatmate and subs
## Abstract The title compounds have been prepared by a simple and economical procedure from the corresponding Bocprotected Ξ±βbenzyl esters and [^15^N]ammonia with N,Nβ²βcarbonyldiimidazole as coupling agent. Catalytic hydrogenolysis furnished both labelled products in high overall yields suitable f