81779-27-3Relevant articles and documents
A PRACTICAL AND SHORT ACCES TO 4-HYDROXY-3-INDOLECARBALDEHYDE AND ITS APPLICATION FOR THE SYNTHESIS OF PINDOLOL ANALOG
Somei, Masanori,Iwasa, Etsuo,Yamada, Fumio
, p. 3065 - 3069 (1986)
4-Hydroxy-3-indolecarbaldehyde (1) is produced simply by heating (3-formylindol-4-yl)thallium bis-trifluoroacetate with copper sulfate in N,N-dimethylformamide and water.Alkylation of 1 afforded predominantly 1-alkyl derivatives.Utilizing these results pindolol analog, 1-allyl-4-(3-t-butylamino-2-hydroxypropoxy)-3-indolecarbaldehyde was synthesized.
TRICYCLIC INDOLE COMPOUNDS HAVING AFFINITY FOR SEROTONIN RECEPTOR
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, (2008/06/13)
Having an affinity against serotonine receptors, compound (I) shown below is useful as a therapeutic agent against various kinds of diseases of central nervous systems. (wherein R1 is hydrogen ; R2 is hydrogen or lower alkyl ; R
Preparations of 1-hydroxyindole derivatives and their potent inhibitory activities on platelet aggregation
Somei, Masanori,Yamada, Koji,Hasegawa, Masakazu,Tabata, Mutsuko,Nagahama, Yoshiyuki,Morikawa, Harunobu,Yamada, Fumio
, p. 1855 - 1858 (2007/10/03)
1-Hydroxymelatonin, 5-bromo- and 5,7-dibromo-1-hydroxytryptamine derivatives, 1,4-dihydroxy-5-nitroindole, 1-hydroxy-3-methylsulfinylmethylindole, and 5-acetyl-1,3,4,5-tetrahydro-1-hydroxypyrrolo[4,3,2-de]quinoline were synthesized for the first time. 1-Hydroxyindoles revealed potent inhibitory activities on platelet aggregation.