Improvements have baen made to the synthesis of 5-aminasalicylic wid (S-ASA) in order to make it applicable for the small-scale synthesis of 5-smidcerboxvl-l ~l s a l i c y l i c acid.
A short synthesis of 5-amino[4-14]laevulinic acid hydrochloride
โ Scribed by J B Cambell; J S Johnston
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- French
- Weight
- 219 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0022-2135
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โฆ Synopsis
5-Amin0[4-'~C]laevulinic
acid hydrochloride has been prepared from potassium [14C]cyanide in 56% overall yield. The key step is the palladium[O] catalysed coupling of 2-phthalimid0[l-'~C]acetyl chloride with 2-carboethoxyethylzinc iodide to give 5-phthalimid0[4-'~C]laevulinic acid ethyl ester in 86% yield. The synthesis was carried out at high specific activity from J20mCi of starting material.
๐ SIMILAR VOLUMES
## Abstract A convenient synthesis of the ^14^Cโlabelled chloromethyl ketone analog of leucine is reported. Modification of previously published conditions allowed for the facile synthesis of: 2โ^14^Cโ3โaminoโ1โchloroโ5โmethylhexanโ2โone hydrochloride in four steps from 1โ^14^CโDLโleucine in 85.7%
## Abstract The synthesis of 2,4โdiaminoโ5โphenylthiazole hydrochloride labelled with carbon โ 14 in the 2โposition has been effected whereby the ^14^Cโlabel was introduced in the last step. The overall yields were 34.5% (gravimetrically) and 32.8% (radiochemically).
## Synthesis of the title compound ( 5 ) . an histamine H2 -receptor antagonist, is described. Treatment of 3-(3-[2.6-C1-piperidinomethylphenoxv)propylamine(l)l with 3-amino-4-methoxy-l,2,5-thiadiazole-1-oxide2 produced 3-amino-4-13-0-[ 2,6-"C]piperidinomethylphenoxy)propylamino~-1,2,5-thiadiazole