## Abstract NβPhenylβ2βnaphthylamine has been synthesized (1) with ^14^C in positions 1, 4, 5 and 8, (2) with ^13^C in position 8 (small amounts of [1β^13^C] naphthalene and 2β[8β^13^C]naphthylamine are formed as byβproducts), and (3) with the Nβphenyl nucleus uniformly labelled with ^14^C.
Synthesis of N-[4-[2-(2,4-dimethylphenoxy)phenyl]-2-thiazolyl]-hexahydro-2-pyrimidinimine, [14C]BAY w 6341
β Scribed by Ulrich Pleiss; Michael Conrad; Bernd Baasner
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- French
- Weight
- 211 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0022-2135
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β¦ Synopsis
Abstract
The title compound [^14^C]BAY w 6341 was synthesized as part of a 4βstep sequence. Starting from diethyl [2β^14^C]malonate the final product (8) was obtained with a specific activity of 1.2 GBq/mmol (32.9 mCi/mmol) and a radiochemical purity of > 99 % in an overall yield of 19 %.
π SIMILAR VOLUMES
We report here a facile synthesis of (RS) methyl-2-([2 0 -14 C]4,6-dimethoxypyrimidin-2 0yloxy)-2-phenyl [1-14 C]ethanoate under microwave irradiation.
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l-(2,6-Difluorobenzoyl)-3-(2-fluoro-4-(2-chloro-4trifluoromethylphenoxy) [ ring-U-14C]phenyl)urea, a potent new acylurea insecticide and acaricide known as flufenoxuron, was labelled with carbon-14 starting from o-dinitro[ring-U-14C]benzene 1. 2-Fl~oronitro[ring-U-~~C]benzene, 2 obtained by fluorina
4-[2-(Di -n-pr yl amino)et hyl l-2 (3H)-indolone ( 1 ) labeled with ? !C at C2 was prepared by a simple and efficient procedure involving carbonation o f a stabilized benzvllithium species. fol owed by ring closure under hydrolytic conditions.