Preparation of 1,2-dimethoxy-4-(bis-diethylaminoethyl-[14C]-amino)-5-bromobenzene
✍ Scribed by Theodore S. T. Wang; Rashid A Fawwaz; Ronald H. van Heertum
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- French
- Weight
- 224 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
1,2‐Dimethoxy‐4‐(bis‐diethylaminoethyl‐[^14^C]‐amino)‐5‐bromobenzene (III) was synthesized for in vivo pharmacokinetic and pharmacodynamic evaluation. The synthesis of (III) was easily obtained by the direct alkylation of 1,2‐dimethoxy‐5‐bromo‐aniline with beta‐diethylaminoethyl chloride‐ethylene‐[^14^C], using CH~3~MgCl as the proton abstractor. Compound III was obtained with a 22.3% yield. The specific activity was 2.2mCi/mmol, with a radiochemical purity of >99%.
📜 SIMILAR VOLUMES
## Abstract 2,2′,5′,2″– [2′,5′ – ^14^C~2~] Terthienyl and 1,4–Bis (2–Thienl) [1,4–^14^C~2~] butadiyne were synthesized from [14~C~] formic acid.
Jusohonmachi 2-chomer Yodogawa-ku, Osaka? Japan SUMMARY 6-( 10-Hydroxy-[l-14Cldecyl) -2,3-dimethoxy-5-methyl-1,4-benzoquinone (VIII) having a specific activity of 23.4 mCi/mmol was synthesized. 9-(2-Hydroxy-3,4-dimethoxy-6methyl-[ carbonyl-4C]benzoyl) nonanol (VI) was obtained from the condensation