4,4'-(Methylene-'T)bis[ N, N-dimethylbenzenamine] (3, 2,4-'4C, 6-trimethylbenzenamine hydrochloride (3, and 4-chlor0-2-(methyl-~~C)benzenarnine hydrochloride (3 were synthesized for an investigation of the metabolism of carcinogenic compounds. Evaluations of synthetic routes led to the following pre
Synthesis of 14C-labelled isopropyl, diisopropyl and methyldiisopropyl amine
✍ Scribed by C. Colombini; M. Terbojevich; E. Peggion
- Publisher
- John Wiley and Sons
- Year
- 1965
- Tongue
- French
- Weight
- 304 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Isopropyl, diisopropyl and methyldiisopropyl aminey, specijically labeled with 14C in the isopropyl moiety, have readily been prepared at a good yield, starting from Acetone-2-1dC. Isopropylamine-2-14C
[111] at 10 mC/mM was obtained by a two step synthesis with a 75 % overall yield based on Acetone-2-14C. Diisopropylamine-2-l4C [VI] at 3 mC/mM was prepared in a two step synthesis in 61 overall yield. From [VI], methyldiisopropylamine-2-14C [VII] at I mCfmM was obtained in one step at a 93 % yield.
Starting with various ketones, it is possible to carry out radiosynteses of homologous primary, secondary and tertiary amines according to the described reaction schemes.
📜 SIMILAR VOLUMES
N-Nitrosobis(2-hydroxypropy1)amine (BHP potent pancreatic carcinogen in the Syrian golden hamster, was synthesized with the 14C-label in the 1-position of one of the propyl groups. Starting with lactic-l-14C acid, RHP was prepared utilizing a four-step reaction sequence, with an overall yield of 45%
## Abstract N‐Nitrosobis (2‐oxopropyl) amine (BOP), a potent and selective pancreatic carcinogen in the Syrian golden hamster was synthesized with a ^14^C label in the alpha carbon. Oxidation of 2‐hydroxypropyl‐2‐hydroxypropyl‐1‐^14^C‐amine followed by nitrosation with sodium nitrite and hydrochlor
## Abstract Org 37462 (1) is the active ingredient in Orgalutran^®^, an innovative product that reduces the time of treatment in __in vitro__ fertilization from four to less than two weeks. Org 37462 is a synthetic decapeptide containing several amino acids that are unnatural in stereochemistry and
## Abstract ^13^C‐ and ^14^C‐uniformly labelled catechol was synthesized from phenol in three steps. Phenol was derivatized with 2‐chloro‐5‐nitrobenzophenone in THF containing NaH, followed by __ortho__‐hydroxylation with 35% aqueous H~2~O~2~ in sulphuric acid/glacial acetic acid solution, and by c