A SYNTHETIC ROUTE TO 3-(DIALKYLAMINO)PHENOTHIAZIN-5-IUM SALTS AND 3,7-DISUBSTITUTED DERIVATIVES CONTAINING 2 DIFFERENT AMINO-GROUPS

Authors
STREKOWSKI L HOU DF WYDRA RL SCHINAZI RF
Citation
L. Strekowski et al., A SYNTHETIC ROUTE TO 3-(DIALKYLAMINO)PHENOTHIAZIN-5-IUM SALTS AND 3,7-DISUBSTITUTED DERIVATIVES CONTAINING 2 DIFFERENT AMINO-GROUPS, Journal of heterocyclic chemistry, 30(6), 1993, pp. 1693-1695
Citations number
7
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of heterocyclic chemistry → ACNP
ISSN journal
0022152X
Volume
30
Issue
6
Year of publication
1993
Pages
1693 - 1695
Database
ISI
SICI code
0022-152X(1993)30:6<1693:ASRT3S>2.0.ZU;2-M
Abstract
Phenothiazin-5-ium tetraiodide hydrate (2), the suggested oxidation pr oduct of phenothiazine with iodine, is treated with two equivalents of a dialkylamine to give 3-(dialkylamino)phenothiazin-5-ium triiodides, 3-6. 3,7-Disubstituted phenothiazin-5-ium iodides, 7-9, are obtained by the reaction of 3-6 with an amine.