Hongxia Han

Efficient One‐Pot Synthesis of 2‐Amino‐4,6‐diarylbenzene‐1,3‐dicarbonitrile under Solvent‐Free Conditions

Abstract A facile parallel synthesis of 2‐amino‐4,6‐diarylbenzene‐1,3‐dicarbonitrile derivatives via a one‐pot reaction of aromatic aldehydes, aromatic ketone, and malononitrile under solvent‐free conditions has been developed. This new protocol has the advantages of shorter time, higher yields, lower cost, and environmental friendliness.

Efficient NaOH-Catalyzed Reaction of Aromatic Aldehyde, Cyclic Ketones, and Malononitrile Under Solvent-Free Conditions Using a Grinding Method

Abstract An efficient and facile synthesis of 2,6-dicyanoanilines via a one-pot reaction of aromatic aldehydes, malononitrile, and cyclic ketones in the presence of NaOH under solvent-free conditions using a grinding method has been developed. Compared with the classical reaction conditions, the new synthetic method has the advantages of excellent yields, shorter reaction times, and mild reaction conditions.

One‐Pot Synthesis of 4,6‐Diaryl‐2‐oxo‐1,2‐dihydropyridine‐3‐carbonitriles via Three‐Component Cyclocondensation under Solvent‐Free Conditions

Abstract An efficient and facile synthesis of 4,6‐diaryl‐2‐oxo‐1,2‐dihydropyridine‐3‐carbonitriles via three‐component cyclocondensation from aromatic aldehydes, aromatic ketones, and 2‐cyanoacetamide under solvent‐free conditions is described. The mild reaction conditions, simple protocol, and clean reaction make this protocol practical and economically attractive.

Efficient and Facile Synthesis of 3-Amino-1-aryl-9H-fluorene-2,4-dicarbonitrile Under Solvent-Free Conditions

Abstract A versatile and efficient route to 3-amino-1-aryl-9H-fluorene-2,4-dicarbonitrile via multicomponent reactions of 1-indanone, aromatic aldehydes, and malononitrile under solvent-free conditions using NaOH as the catalyst is described. This method provides several advantages over alternative procedures such as mild, solvent-free conditions at ambient temperature and direct isolation of the products in good yields.

EFFICIENT SYNTHESIS OF 6-AMINO-8-ARYL-2-METHYL-1,2,3,4-TETRAHYDROISOQUINOLINE-5,7-DICARBONITRILE UNDER SOLVENT-FREE CONDITIONS

A series of 6-amino-8-aryl-2-methyl-1,2,3,4-tetrahydroisoquinoline-5,7-dicarbonitriles were prepared in good yields under solvent-free conditions by multicomponent reactions of aromatic aldehyde, malononitrile, and 1-methylpiperidin-4-one in the presence of sodium hydroxide (NaOH). The structures of the products were characterized by infrared, 1H NMR spectra, elemental analysis, and high-resolution mass spectrometery (HRMS).

Efficient One-Pot Synthesis of 4-Aryl-3-cyano-2,5-dihydro-1H-indeno[1,2-b]pyridin-2-one and 4-Aryl-3-cyano-1,2,5,6-tetrahydrobenzo[h]quinolin-2-one Derivatives Under Solvent-Free Conditions

Abstract 4-Aryl-3-cyano-2,5-dihydro-1H-indeno[1,2-b]pyridin-2-one and 4-aryl-3-cyano-1,2,5,6-tetrahydrobenzo[h]quinolin-2-one have been prepared from indan-1-one or 3,4-dihydronaphthalen-1(2H)-one, aromatic aldehydes, 2-cyanoacetamide, in the presence of sodium hydroxide under solvent-free conditions. The rapid and facile method produced products in high yields.

Efficient and Facile Synthesis of 2,4-Diamino-6-arylpyrimidine-5-carbonitrile Under Solvent-Free Conditions

An efficient and convenient method for the preparation of 2,4-diamino-6-arylpyrimidine-5-carbonitrile derivatives by the one-pot reaction of aromatic aldehydes, malononitrile, and guanidine carbonate, in the presence of sodium hydroxide under solvent-free conditions, was reported. This method has the advantages of excellent yields, mild reaction conditions, easy work up, and environmental friendliness over the existing procedures.

Efficient and Facile Three-Component Reaction for the Synthesis of 2-Amine-4,6-diarylpyrimidine Under Solvent-Free Conditions

Abstract An efficient and convenient multicomponent reaction for the preparation of 2-amine-4,6-diarylpyrimidine by aromatic aldehydes, aromatic ketones, and guanidine carbonate in the presence of sodium hydroxide under solvent-free conditions is reported. The short reaction time coupled with the simplicity of the reaction procedure make this method one of the most efficient methods for the synthesis of this class of compounds.

Solvent‐Free Synthesis of 3‐Amino‐2,4‐dicarbonitrile‐5‐methylbiphenyl by a Grinding Method

Abstract A convenient, environmentally friendly, and solvent‐free procedure has been developed for the synthesis of 3‐amino‐2,4‐dicarbonitrile‐5‐methylbiphenyl derivatives. Compared with the classical reaction condition, this new synthetic method has the advantages of excellent yields, easy setup, mild reaction conditions, and environmental friendlines.