## Abstract The synthesis of [^15^N]‐ labelled procaine hydrochloride, using (^15^NH~4~)~2~SO~4~ as starting isotopically labelled material, is presented. The experimental procedure is an adaptation of the synthesis methods for the corresponding unlabelled compounds.
Synthesis of [15N]t-butylamine hydrochloride
✍ Scribed by Yingdan Zhang; Chaojie Lin; Zhan Li; Liqiong Qin; Hongliang Wen
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- French
- Weight
- 86 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
This report presents an efficient synthesis of [^15^N]t‐butylamine hydrochloride. Acylation of [^15^N]ammonia with pivaloyl chloride provided [^15^N]pivalamide, this was converted to benzyl [^15^N]N‐t‐butylcarbamate through a Hofmann rearrangement. Hydrogenolysis of benzyl [^15^N]N‐t‐buylcarbamate and acidification afforded [^15^N]t‐butylamine hydrochloride in an overall yield of 79.2% in four steps. Copyright © 2010 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
## Abstract 1‐[^15^N]Amino‐2‐propanol hydrochloride (**2**) was synthesized in three steps, i.e. Gabriel condensation of potassium [^15^N]phthalimide (**3**) with chloroacetone (**4**), reduction of the product ([^15^N]phthalimidoacetone (**5**)) with sodium borohydride, and hydrolysis in 33% total
## S u in ma r y 1sN.15N-imidazoleacetic acid was synthesized from 15N, lSN-DL-histidine (>99 atom % 15N). The latter. oxidized with sodium hypochlorite. formed 15N.15N-imidazoleacetoniuile. The free acid was prepared after acid hydrolysis of the nitrile, elution from an anion exchange column with
Coniine-15N was obtained by the reductive amination of 5-0x0octanal using sodium cyanoborohydride and a m m o n i ~m -~~N bromide. Nornicotine-l'-15N resulted from a similar reductive aminution of 4-oxo-4-(3'-pyridyl)butanal. Merhybtion with formaldehyde and ,formic acid afforded n i ~o t i n e -I '