## Abstract Carbon‐14 labeled 4‐[4‐[2‐[2‐[bis(4‐chlorophenyl)methoxyethylsulfonyl] [1‐^14^C]ethoxy]phenyl]‐1,1,1‐trifluoro‐2‐butanone was prepared in a six step radioactive synthesis from 2‐bromo[1‐^14^C]acetic acid. The overall radiochemical yield was 2.2%. The specific activity of the final produ
Synthesis and purification of carbon-14 labelled 1, 1-hexamethylene-bis [5-(4-chlorophenyl)biguanide] (chlorhexidine), ‘Hibitane’
✍ Scribed by J. Burns
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- French
- Weight
- 425 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
Two syntheses of [^14^C] chlorhexidine (‘Hibitane’) with the label specifically incorporated in two separate molecular positions are described. Ring labelled chlorhexidine prepared from p‐chloro[U‐14C]aniline was obtained with a molar specific activity of 27.9 mCi/mmol. Chain labelled material, where the ^14^C label was incorporated in the 1 and 6 positions of the hexamethylene bridge, was prepared from [1, 6 ^14^C]‐adiponitrile, with a molar specific activity of 11.5 mCi/mmol. Several methods of purification are described.
📜 SIMILAR VOLUMES
Phenyl-piperazinomethyl-amino-oxazoline 3. labelled with carbon-14 was obtained in good yield in two steps from [14CIepichlorhydrin. Specific radioactivity: 19.40 PCilmg; 5,09 mCilmmo1. Radiochemical yield: 50 % of the theoretical amount.
## Abstract The synthesis of ^14^C‐labelled __cis__‐malonato[(4__R__,5__R__)‐4,5‐bis(aminomethyl)‐2‐isopropyl‐1,3‐dioxolane]platinum(II) from [1,4‐^14^C] D‐tartaric acid is described. The overall radiochemical yield of the product in a eight‐step sequence was 23.8% and radiochemical purity was 98.5
The synthesis in eight steps of the title compound from the commercially available[2O-"C]pregnenolone 1 is described. ## The expected I-[4-methyl-3-oxo-4-aza-5a-androstane-17~-[14C]carbonyl]-1,3-diisopropylurea ([14C]FCE 26073) was obtained with a radiochemical purity higher than 97% and a specif
## Abstract This paper describes the synthesis and characterisation of 2[[4‐(2,6‐di‐1‐pyrrolidinyl‐4‐pyrimidinyl)‐1‐piperazinyl]‐[^14^C]‐ methyl]‐3,4‐dihydro‐2,5,7,8‐tetramethyl‐2H‐1‐benzopyran‐6‐ol and 2[[4‐(2,6‐di‐1‐pyrrolidinyl‐4‐[^13^C~2~]‐pyrimidinyl)‐1‐ piperazinyl]‐[^13^C]‐methyl]‐3,4‐dihydr