摘要:
THE INVENTION RELATES TO NOVEL 1-(4-R1O-PHENYL)-2-(4R2-PHENYL)-6-R3-1,2,3,4-TETRAHYDROQUINOLINES HAVING ANTIFERTILITY AND HYPOCHOLESTEROLEMIC ACTIVITES, TO THEIR PREPARATION, AND TO NOVEL INTERMEDIATES THEREFOR.
摘要:
THE COMPOUND ARE HEXAHYDRO, OCTAHYDRO AND DECAHYDRO IMIDAZO (2,1-)QUINAZOLINES AND PYRIMIDO (2,1-B) QUINAZOLINES WHICH HAVE HYPOTENSIVE ACTIVITY. FOR EXAMPLE, COMPOUNDS OF THIS INVENTION ARE 1,2,3,5,6,7,8,9-OCTAHYDRO-6H-PYRIMIDO (2,1B) QUINAZOLINE AND 1,2,34,7,8,9,10-OCTAHYDRO-6-H-PYRIMIDO (2,1-B) QUINAZOLINE.
摘要:
2,3 - DIHYDRO - 2 - (1-NAPHTHYL) - 4(1H)QUINAZOLINONE AND THE 6 - CHLOROANALOG ARE PROVIDED BY THIS INVENTION. THESE COMPOUNDS ARE USEFUL IN CONTROLLING FERTILITY IN WARM-BLOODED MALE ANIMALS.
INCLUDING THE PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF, IN WHICH X IS HALOGEN OR TRIFLUOROMETHYL; R6 AND R6'' ARE LOWERALKYL, PHENYL, OR PHENYLLOWERALKYL; OR R6 IS HYDROGEN AND R6'' IS ACYL SUCH AS ACETYL OR C3H7CO, OR PHENYLLOWERALKYL OR PHENYLLOWERALKYL; R2 AND R2'' ARE HYDROGEN, LOWERALKYL, LOWERALKENYL, THIOLOWERALKYL, ALKYLTHIO, HALOGEN SUBSTITUTED LOWERALKYL, PHENYLALKYL, PHENYL, CYCLOALKYL, CYCLOALKYLLOWERALKYL, LOWERALKOXY, LOWERALKOXYLOWERALKYL, OR R2 AND R2'' TOGHETHER ARE LOWER POLYMETHYLENE CHAIN MORPHOLINO, PYRROLIDINO, OR PIPERAZINO; R1 IS HYDROGEN, PHENYLALKYL, HYDROXYALKYL, LOWERALKOXYLOWERALKYL, OR LOWERALKYL; R5 AND R8 ARE HYDROGEN, LOWERALKYL, AMINO, LOWERALKOXY, OR LOWERALKOXYLOWERALKYL; R3, R3'', AND R3" ARE HYDROGEN, LOWERALKYL, HYDROXY, LOWERALKOXY, LOWERALKOXYLOWERALKYL, HALOGEN, TRIFLUOROMETHYL, SULFAMYL, OR AMINO, AND N IS AN INTEGER FROM 0-4.
摘要:
Processes that use novel reagents for the removal of colored impurity during the preparation of Salcaprozic Acid and pharmaceutically acceptable salts thereof. The processes include hydrolysis of 8-(2,4-dioxo-1,3-benzoxazin-3-yl)octanoic acid ethyl ester in the presence of or by contacting it with benzotriazole, hydrazine and/or sodium borohydride.
摘要:
Described herein are novel methods of synthesizing 2-amino-5-chloro-N,3-dimethylbenzamide. Compounds prepared by the methods disclosed herein are useful for preparation of certain anthranilamide compounds that are of interest as insecticides, such as, for example, the insecticides chlorantraniliprole and cyantraniliprole.
摘要:
The invention provides compounds and compositions comprising compounds that modulate histone acyl transferase (HAT). The invention further provides methods for treating neurodegenerative disorders, conditions associated with accumulated amyloid-beta peptide deposits, Tau protein levels, and/or accumulations of alpha-synuclein as well as cancer by administering a compound that modulates HAT to a subject.
摘要:
Isatoic anhydride derivatives having an N-substituent which includes a quaternary ammonium group are useful for labeling and/or functionalizing a target material and/or for coupling materials together. The isatoic anhydride derivatives of the present disclosure can be advantageously water soluble, easily prepared and purified. Isatoic anhydride derivatives useful in the present disclosure preferably have at least one chemically reactive group or at least one binding group or at least one detectable label. Anthranilate derivatives made from the isatoic anhydrides derivatives or otherwise and kits including the isatoic anhydride derivatives are also disclosed.