## Abstract The mass spectra and main fragmentation pathways are presented for thirteen 1‐ and 3‐substituted 5,5‐diphenylglycocyamidine and ‐hydantoin derivatives. The principal decomposition routes of these compounds are also of diagnostic value for ascertaining positional isomerism when the subst
Preparative resolution of some 5,5-hydantoin derivatives via formation of diastereoisomeric salts
✍ Scribed by Gérard Coquerel; Marie-Noëlle Petit; Roger Bouaziz; Dominique Depernet
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 266 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0899-0042
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✦ Synopsis
Several preparative resolutions of 5,5-disubstituted hydantoins have been achieved via fractional crystallization of diastereoisomeric salts. The process can be extended by making use of the difference between the variation of solubilities of the hydantoins and their salts with a-methylbenzylamine as a function of the alkalinity of the medium. Optimization for each resolution procedure involves a refinement of the excess amount of base needed.
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Racemic N-methylamphetamine can be resolved by O,OЈ-di-ptoluoyltartaric acid in methanol either by the classic Pasteurian method by fractional crystallization of the neutral diastereoisomeric salt pair (molar ratio of the base:acid 2:1) or by the Marckwald or the Pope-Peachey method by fractional cr
## Abstract PI salts condense with 1, 3‐dimethyl barbituric acid and 1, 3‐dimethyl‐4 ‐amino uracil to give new amide chlorides 4 and 5. These synthons lead to new aminated isoxazolo‐, or pyrimido‐ and pyrido‐pyrimidines 12, 16 & 18 on cyclisation with hydroxylamine, cyanamide and malononitrile, res