253440-88-9Relevant articles and documents
INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE AND/OR TRYPTOPHAN 2,3-DIOXYGENASE
-
Page/Page column 46-47, (2021/01/29)
The present invention relates to compounds of Formula (I) inhibiting indoleamine 2,3-dioxygenase (IDO) and/or tryptophan 2,3-dioxygenase (TDO) enzymes. Further, their synthesis and their use as medicaments in the treatment of inter alia cancer is disclose
CONDENSED HETEROCYCLIC COMPOUND HAVING CYCLOALKYLPYRIDYL GROUP OR SALTS THEREOF, INSECTICIDE FOR AGRICULTURE AND HORTICULTURE CONTAINING THE COMPOUND, AND METHOD FOR USING THE INSECTICIDE
-
Paragraph 0111, (2017/12/15)
PROBLEM TO BE SOLVED: To provide a new insecticide for agriculture and horticulture, in consideration of factors such as the occurrence of vermin resistant to existing insecticides, as the damage caused by vermin etc. is still serious in crop production such as agriculture and horticulture. SOLUTION: This invention provides: a condensed heterocyclic compound that has a cycloalkylpyridyl group expressed by formula (1), or salts thereof; an insecticide for agriculture and horticulture containing the compound; and a method for using the insecticide. {R1 is a haloalkyl group; A1 is O or an N-methyl group; A2 and A3 are a CH group or N; Ra, Rb, and Rc are H; m is an integer of 0-2; and n is 1 or 2}. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT
Mild fluorination of chloropyridines with in situ generated anhydrous tetrabutylammonium fluoride
Allen, Laura J.,Muhuhi, Joseck M.,Bland, Douglas C.,Merzel, Rachel,Sanford, Melanie S.
, p. 5827 - 5833 (2014/07/08)
This paper describes the fluorination of nitrogen heterocycles using anhydrous NBu4F. Quinoline derivatives as well as a number of 3- and 5-substituted pyridines undergo high-yielding fluorination at room temperature using this reagent. These results with anhydrous NBu4F compare favorably to traditional halex fluorinations using alkali metal fluorides, which generally require temperatures of ≥100 °C.