154386-63-7

Usage

Specific substituent

2-iodophenyl
Two methyl groups attached to the nitrogen atom
Commonly used in chemical and pharmaceutical research as a reactant or substrate in organic synthesis
Potential applications in medicinal chemistry, material science, and agriculture
Building block for the synthesis of biologically active molecules and functional materials

Upstream product

• 108501-85-5 N-(2-iodophenyl)-2-methylacrylamide 
• 74-88-4 methyl iodide 
• 615-43-0 2-iodophenylamine 
• 74-83-9 methyl bromide 
• 100-61-8 N-methylaniline 
• 62-53-3 aniline 

Downstream Products

• 75116-29-9 3-(2-(4-methoxyphenyl)-2-oxoethyl)-1,3-dimethylindolin-2-one 
• 1240239-75-1 (E)-1,3-dimethyl-3-styrylindolin-2-one 
• 1454769-90-4 (E)-1,3-dimethyl-3-(2'-methylstyryl)indolin-2-one 
• 1454769-91-5 (E)-3-1,3-dimethyl-(2’-methoxystyryl)indolin-2-one 
• 1454769-92-6 (E)-1,3-dimethyl-3-(2'-bromostyryl)indolin-2-one 
• 1454769-93-7 (E)-1,3-dimethyl-3-(4'-chlorostyryl)indolin-2-one 
• 1454769-94-8 (E)-1,3-dimethyl-3-(4'-methoxystyryl)indolin-2-one 
• 1454769-95-9 (E)-1,3-dimethyl-3-(4'-tert-butylstyryl)indolin-2-one 
• 1454769-96-0 (E)-1,3-dimethyl-3-(4'-ethoxycarbonylstyryl)indolin-2-one 
• 1454769-97-1 (E)-1,3-dimethyl-3-(4'-cyanostyryl)indolin-2-one 
• 1454769-98-2 (E)-1,3-dimethyl-3-(3'-nitrostyryl)indolin-2-one 
• 1603104-71-7 1,3-dimethyl-3-(3-phenylprop-2-yn-1-yl)indolin-2-one 
• 1603105-62-9 1,2a-dimethyl-5-phenyl-2a,3-dihydrobenzo[cd]indol-2(1H)-one 
• 1603104-72-8 1,3-dimethyl-3-(3-(p-tolyl)prop-2-yn-1-yl)indolin-2-one 

Relevant academic research and scientific papers

Iodine-Promoted Metal-Free Cyclization and O/S Exchange of Acrylamides with Thiuram: One-Step Synthesis of Quinolino-2-thiones

A one-step cyclization and O/S exchange reaction of readily available acrylamides in the presence of iodine and thiuram has been developed. The reaction provides an efficient approach for the synthesis of highly important heterocycle quinolino-2-thiones with diverse substitution patterns.

Palladium-Catalyzed Enantioselective Intramolecular Heck Carbonylation Reactions: Asymmetric Synthesis of 2-Oxindole Ynones and Carboxylic Acids

Herein, we report a Pd-catalyzed enantioselective domino Heck carbonylation reaction of o-iodoacrylanilides with terminal alkynes and water as the nucleophiles, affording a diversity of β-carbonylated 2-oxindole derivatives bearing a 3,3-disubstituted all-carbon quaternary stereocenter, in high yields (55–99 %) with good to excellent enantioselectivities (up to 99 % ee). The synthetic utilities of the protocol were demonstrated in the gram-scale synthesis of 2-oxindole-derived ynone 3 ea and carboxylic acid 4 a, as well as the facile synthesis of chiral 2-oxindoles with a pyrazole or isoxazole moiety.

Palladium-Catalyzed Domino Heck/Sulfination: Synthesis of Sulfonylated Hetero- And Carbocyclic Scaffolds Using DABCO-Bis(sulfur dioxide)

The synthesis of a broad variety of hetero- and carbocyclic scaffolds via a Pd-catalyzed domino Heck/SO2 insertion reaction is reported. This reaction utilizes DABSO, a safe and easy-to-handle alternative to SO2 gas. The reaction proceeds through a sulfin

Palladium-Catalyzed Domino Synthesis of 2,3-Difunctionalized Indoles via Migratory Insertion of Isocyanides in Batch and Continuous Flow

We report, herein, a palladium-catalyzed cascade comprising carbopalladation, migratory insertion of isocyanide and triple bond activation followed by a nucleophilic attack (OR?) to construct difunctionalized acyl indoles. The process involves

Nickel-Catalyzed Arylcarbamoylation of Alkenes of N-(o-Iodoaryl)acrylamides with Nitroarenes via Reductive Aminocarbonylation: Facile Synthesis of Carbamoyl-Substituted Oxindoles

Nickel-catalyzed arylcarbamoylation reactions of alkenes of N-(o-haloaryl)acrylamides with CO and nitroarenes via reductive aminocarbonylation to produce carbamoyl-substituted oxindoles with an all-carbon quaternary stereogenic center are presented. Starting with N-(o-haloaryl)acrylamides, simple CO, and inexpensive nitroarenes and using a Ni catalyst, a dinitrogen-based ligand, a Zn reductant, a TMSCl additive, and a base system, this protocol enables the synthesis of various carbamoyl-substituted oxindoles and allows the efficient late-stage derivatization of valuable molecules.

3,3′-Disubstituted Oxindoles Formation via Copper-Catalyzed Arylboration and Arylsilylation of Alkenes

Arylboration and arylsilylation reactions of N-(2-iodoaryl)acrylamides with bis(pinacolato)-diboron (B2pin2) or PhMe2Si-Bpin are developed by using simple CuOAc as the sole catalyst. A range of boron-or silane-bearing 3,3′-disubstituted oxindoles are obtained in moderate to excellent yields. The reaction is proposed to proceed via a domino sequence involving intermolecular olefin borylcupration or silylcupration followed by intramolecular coupling of an alkyl-Cu intermediate with aryl iodide.

Nickel-catalyzed reductive aryl thiocarbonylation of alkene via thioester group transfer strategy

Herein reported is a nickel-catalyzed reductive aryl thiocarbonylation of alkene via thioester group transfer strategy by using simple and readily available thioesters. In contrast to traditional activation of weaker C(acyl)-S bond, the C(acyl)-C bond of

Pd/Cu-Catalyzed Enantioselective Sequential Heck/Sonogashira Coupling: Asymmetric Synthesis of Oxindoles Containing Trifluoromethylated Quaternary Stereogenic Centers

An asymmetric palladium and copper co-catalyzed Heck/Sonogashira reaction between o-iodoacrylanilides and terminal alkynes to synthesize chiral oxindoles was developed. In particular, a wide range of CF3-substituted o-iodoacrylanilides reacted

Domino [Pd]-Catalysis: Heck followed by decarboxylative Sonogashira couplings under microwave irradiation in aqueous medium

A copper free [Pd]-catalyzed domino intramolecular Heck and intermolecular decarboxylative Sonogashira couplings, for the synthesis of alkyne bearing heterocyclic compounds with a quaternary carbon atom, is described. Notably, this dual bond forming strategy is successful in water solvent, under microwave irradiation. This one-pot operation enabled the formation of a variety of dihydrobenzofurans, indolines and oxindoles, in very good to near quantitative yields. Notably, unlike earlier reports, the present strategy is successful in delivering the products with short alkyl substituents on acetylene carbon, which is first of its kind.

Microwave-Assisted Domino Heck Cyclization and Phosphorylation: Synthesis of Phosphorus Containing Heterocycles

A domino [Pd]-catalyzed intramolecular Heck cyclization followed by intermolecular phosphorylation, for the construction of phosphorus containing heterocyclic compounds, is presented. Notably, the process is accelerated by microwave heating conditions and enabled the construction of C–C and C–P bonds in short reaction times.