22258-71-5Relevant articles and documents
On interaction of 2-amino-benzothiazoles with halohydrins
Ambartsumova
, p. 860 - 865 (1999)
Interaction of 2-aminobenzothiazoles with ethylene chlorohydrin on boiling leads mainly to formation of the corresponding 3-(β-chloroethyl)benzothiazolin-2-ones. Reducing the reaction temperature increases the fraction of 2-imino-(3-β-hydroxyethyl)benzothiazolines. In both instances formation of bis[3-(β-hydroxyethyl)benzothiazol-2-ylidene]ammonium chlorides is observed. The reaction of 2-aminobenzothiazole with propylene bromohydrin gives only the corresponding amino alcohols. The anomalous products from the reaction of β-chloroethyl derivatives of benzothiazolinones result from a dominating side reaction of the starting 2-aminobenzothiazoles with the ethylene chlorohydrin thermolysis products that are formed on boiling. 1999 KluwerAcademic/Plenum Publishers.
Benzimidazolidinone derivatives as muscarinic agents
-
Page/Page column 19, (2010/02/06)
Benzimidazolidinone derivative compounds, which increase acetylcholine signaling or effect in the brain, and highly selective muscarinic agonists, particularly for the M1 and/or M4 receptor subtypes, pharmaceutical compositions comprising the same, as well as methods of treating psychosis using these compounds are disclosed.
BEHAVIOR OF ETHYLENE CHLOROHYDRIN IN REACTIONS WITH 2-AMINOBENZOTHIAZOLES
Ambartsumova, R. F.
, p. 1932 - 1933 (2007/10/02)
-