An efficient and green synthesis of highly functionalized N-methyl-2-nitro-aryl-1H-benzo[f]chromen-3-amine derivatives under catalyst-free conditions
-
Add time:07/17/2019 Source:sciencedirect.com
A highly efficient and environmentally benign protocol has been developed for the construction of various potentially biologically active N-methyl-2-nitro-aryl-1H-benzo[f]chromen-3-amine derivatives using one-pot, multi-component cascade reaction of various naphthalen-2-ol, aldehydes, and (E)-N-methyl-1-(methylthio)-2-nitroethenamine under catalyst-free conditions in the presence of green solvent medium (ethanol–water) is described. The significant features of this protocol are short reaction times, provide excellent yields, avoidance of toxic solvents and catalysts, no column chromatographic purification, atom-economy and uses ethanol–water as a green solvent which is considered to be relatively environmentally benign. This is the first example of the condensation of naphthalen-2-ol, aldehydes, and (E)-N-methyl-1-(methylthio)-2-nitroethenamine to provide a novel series of 1H-benzo[f]chromen-3-amine derivatives.
We also recommend Trading Suppliers and Manufacturers of N-(3-bromophenyl)-N-(3-(3-bromophenyl)-4-(4-methoxyphenyl)-1,3-thiazol-2(3H)-ylidene)amine (cas 385397-80-8). Pls Click Website Link as below: cas 385397-80-8 suppliers
Prev:One-pot and regioselective synthesis of polysubstituted 3,4-dihydroquinazolines and 4,5-dihydro-3H-1,4-benzodiazepin-3-ones by sequential Ugi/Staudinger/aza-Wittig reaction
Next:Simultaneous dehydrogenation and hydrogenolysis of aromatic alcohols in one reaction system via visible-light-driven heterogeneous photocatalysis) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- One-pot and regioselective synthesis of polysubstituted 3,4-dihydroquinazolines and 4,5-dihydro-3H-1,4-benzodiazepin-3-ones by sequential Ugi/Staudinger/aza-Wittig reaction07/16/2019
- Sulfonated graphene oxide-catalyzed N-acetylation of amines with acetonitrile under sonication07/15/2019
- Unusual formation of novel highly substituted N-(3-indolyl)-imidazoles07/14/2019
- Amberlite IRA-400 Cl resin catalyzed synthesis of secondary amines and transformation into N-((1H-indol-3-yl) (heteroaryl) methyl)-N-heteroaryl benzenamines and bis-indoles via multicomponent reaction07/13/2019
- Ultrasonic promoted catalyst-free N-formylation of amines in neutral ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate07/12/2019
- Sulfur, selenium and tellurium containing amines act as effective carbonic anhydrase activators07/11/2019


