๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

A short synthesis of 5-amino[4-14]laevulinic acid hydrochloride

โœ 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

No coin nor oath required. For personal study only.

โœฆ 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.


๐Ÿ“œ SIMILAR VOLUMES


Synthesis of 5-amino[carboxyl-14C]salicy
โœ Ole Jรธrgensen; Susanne Petersen; Lars Carlsen ๐Ÿ“‚ Article ๐Ÿ“… 1987 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 121 KB

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.

Synthesis of 2โ€“14C-3-amino-1-chloro-5-me
โœ Neil J. Lewis; Jan Hes; Philip Yip; Frederick D. Cazer ๐Ÿ“‚ Article ๐Ÿ“… 1977 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 180 KB ๐Ÿ‘ 1 views

## Abstract A convenient synthesis of the ^14^Cโ€labelled chloromethyl ketone analog of leucine is reported. Modification of previously published conditions allowed for the facile synthesis of: 2โ€“^14^Cโ€3โ€aminoโ€1โ€chloroโ€5โ€methylhexanโ€2โ€one hydrochloride in four steps from 1โ€^14^Cโ€DLโ€leucine in 85.7%

Synthesis of 14C-labelled 2,4,-diamino-5
โœ Jeffrey G. Adams; Paul J. Nicholls; Hywel Williams ๐Ÿ“‚ Article ๐Ÿ“… 1976 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 155 KB

## Abstract The synthesis of 2,4โ€diaminoโ€5โ€phenylthiazole hydrochloride labelled with carbon โ€“ 14 in the 2โ€position has been effected whereby the ^14^Cโ€label was introduced in the last step. The overall yields were 34.5% (gravimetrically) and 32.8% (radiochemically).

Synthesis of 3-amino-4-[3-(3-[2,6-14C]-p
โœ J. E. Swigor; R. T. Standridge; T. A. Montzka; J. D. Matiskella; K. A. Pittman ๐Ÿ“‚ Article ๐Ÿ“… 1988 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 209 KB ๐Ÿ‘ 1 views

## 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