1 -M e t h y l -4 -[ 4 -( 7 -c h l o r 0 -4 -q ~n i n o l y l -[ 3 -~~C 1amino)-benzoyllpiperazine (V) was prepared for pharmacokinetic and pharmacodynamic evaluation. The synthesis of V was accomplished first by a modified Claisen ester condensation reaction of diethyl-[2-14C]-malonate, triethyl or
Synthesis of tritium labeled 1-methyl-4-[4-(7-trifluoromethyl-4-quinolyl)-aminobenzoyl]piperazine and derivatives
✍ Scribed by Richard S. P. Hsi
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- French
- Weight
- 440 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Deuteration of p‐aminobenzoic acid hydrochloride (PAB·HCl) was studied to provide a model for tritiating PAB‐HCl. Tritium labeled PAB·HCl was used as the starting material for the synthesis of tritium labeled 1‐methyl‐4‐[4‐(7‐trifluoromethyl‐4‐quinolyl)aminobenzoyl]piperazine (Ic) and the corresponding 1‐demethyl compound (Id) and 1‐oxide (II).
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