Related Products of 18711-13-2, In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 18711-13-2 as follows.
General procedure: Example 1- Synthesi s of 4,7 dichloroisatin analogs [0176] An appropriate acetophenone and 4, 7-dichloroisat were condensed in the presence of a catalytic amount of diethylamme to prepare the desired compound in quantitative yield. Example compounds: R1 = 4′-CN (PT-1-11); 2′-GCH3 (PT-1-12) ; 3′- OCH3 (PT-1 -18) ; 2 FontWeight=”Bold” FontSize=”10″ ,4′-OCH3 (PT-1-19); 2,.3′-( }( 1 i ¡¤. (PT-1-20); 3′,4OCH3 (PT-1 -21 ); 35’OCH3 (PT-1-22); 2,,3′,4′,-OCH3 (PT-1-23); 3’A 5′-OCH3 (PT-1-13); 4′-OC2H5 (PT-1- 14); 4 -CF3 (PT-1-15); 4′-OCF3 (PT-1-16); 4′-N(CH3)2 (PT-1-17); 4′-OPh (PT-1-60); 4′-SCH3 (PT-1-67); and 4′-C(CH3)2 (PT-1-67).
According to the analysis of related databases, 18711-13-2, the application of this compound in the production field has become more and more popular.
Reference:
Patent; GEORGETOWN UNIVERSITY; TORETSKY, Jeffrey, A.; UREN, Aykut; WO2015/61229; (2015); A1;,
Indoline – Wikipedia,
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