Methyl 2-(1-methyl-3-oxoisoindolin-1-yl)acetate

: In this work, we report a facile access to a 3,3-disubstituted isoindolinone by means of Krapcho decarboxylation reaction of the respective substituted dimethyl malonate derivative. Good isolated yields were obtained under mild reaction conditions. of 3,3-disubstituted derivatives the construction of a quaternary a convenient to 3,3-disubstituted isoindolinones by cascade reactions of 2-acylbenzonitriles several nucleophiles investigation of the reactivity between 2-acetylbenzonitrile and dimethyl malonate a very convenient synthesis of the new compound 1 dimethyl the reactivity of 1 in decarboxylation reaction to a ﬀ the useful molecule methyl 2-(1-methyl-3-oxoisoindolin-1-yl)acetate 2 Krapcho reaction Abstract: In this work, we report a facile access to a 3,3-disubstituted isoindolinone by means of Krapcho decarboxylation reaction of the respective substituted dimethyl malonate derivative. Good isolated yields were obtained under mild reaction conditions.


Introduction
Isoindolinones are important heterocyclic compounds, found in a variety of natural products and in a great number of synthetic biologically active compounds ( Figure 1) [1]. The isoindolinone core is composed of a γ-lactam fused with the benzene ring and can be either unsubstituted, or monoor di-substituted in 3-position [1]. If, on one hand, the synthesis of 3-unsubstituted and 3-mono substituted isoindolinones is widely explored and many protocols are available [1,2] reports about the synthesis of 3,3-disubstituted derivatives are relatively few because the construction of a quaternary carbon is generally more challenging [3,4]. In our recent works, we have developed a convenient access to 3,3-disubstituted isoindolinones by cascade reactions of 2-acylbenzonitriles with several nucleophiles [5,6]. In particular, the investigation of the reactivity between 2-acetylbenzonitrile and dimethyl malonate led to a very convenient synthesis of the new compound 1, dimethyl 2-(1-methyl-3-oxoisoindolin-1-yl)malonate [5], which can be of high interest for further transformations. Therefore, in the present work, we have investigated the reactivity of 1 in decarboxylation reaction to afford the useful molecule methyl 2-(1-methyl-3-oxoisoindolin-1-yl)acetate 2 under Krapcho reaction conditions [7,8].

Introduction
Isoindolinones are important heterocyclic compounds, found in a variety of natural products and in a great number of synthetic biologically active compounds ( Figure 1) [1]. The isoindolinone core is composed of a γ-lactam fused with the benzene ring and can be either unsubstituted, or mono-or di-substituted in 3-position [1]. If, on one hand, the synthesis of 3-unsubstituted and 3mono substituted isoindolinones is widely explored and many protocols are available [1,2] reports about the synthesis of 3,3-disubstituted derivatives are relatively few because the construction of a quaternary carbon is generally more challenging [3,4]. In our recent works, we have developed a convenient access to 3,3-disubstituted isoindolinones by cascade reactions of 2-acylbenzonitriles with several nucleophiles [5,6]. In particular, the investigation of the reactivity between 2acetylbenzonitrile and dimethyl malonate led to a very convenient synthesis of the new compound 1, dimethyl 2-(1-methyl-3-oxoisoindolin-1-yl)malonate [5], which can be of high interest for further transformations. Therefore, in the present work, we have investigated the reactivity of 1 in decarboxylation reaction to afford the useful molecule methyl 2-(1-methyl-3-oxoisoindolin-1yl)acetate 2 under Krapcho reaction conditions [7,8].

Result and Discussion
The convenience of performing decarboxylation of malonate dimethylesters under Krapcho reaction conditions is given by the fact that the methyl acetate derivative is directly obtained under mild conditions [7,8]. On the other hand, the mostly used decarboxylation procedures are based on

Result and Discussion
The convenience of performing decarboxylation of malonate dimethylesters under Krapcho reaction conditions is given by the fact that the methyl acetate derivative is directly obtained under On the other hand, the mostly used decarboxylation procedures are based on the treatment of malonate diesters or β-ketoesters with concentrated HCl at reflux; the respective malonic or β-ketoacids, obtained by hydrolysis under basic conditions, can also undergo decarboxylation under milder reaction conditions. However, in these cases, the final product is a carboxylic acid, while the harsh conditions employed can lead to low yields and decomposition products. The Krapcho protocol is based on the combined effect of a Lewis acid and water in high-boiling, polar aprotic solvents like DMSO (dimethyl sulfoxide), under neutral conditions. In preliminary experiments performed at 100 • C, we did not detect the formation of the product (Table 1, Entry 1). The increase of the reaction temperature at 130 • C led to the formation of the desired product 2. However, the optimized protocol depends also on the control of other two reaction parameters. In particular, at 0.10 molar concentration after 5 h of reaction time we observed about 60% conversion, determined by 1 H NMR on the crude, and 40% isolated yield of 2 (Entry 2). Increasing the reaction time at 18 h, we observed an almost complete disappearance of 1 and a good isolated yield (Entry 3). The reaction was also performed in a more concentrated media (0.20 M), giving similar results in a shorter reaction time (Entry 4). The difference between observed conversion and isolated yield is due in part to loss of product during the extraction with water in the work-up procedure for the removal of DMSO and in part because of some amount of decomposition products. Molbank 2020, 2020, x 2 of 4 the treatment of malonate diesters or β-ketoesters with concentrated HCl at reflux; the respective malonic or β-ketoacids, obtained by hydrolysis under basic conditions, can also undergo decarboxylation under milder reaction conditions. However, in these cases, the final product is a carboxylic acid, while the harsh conditions employed can lead to low yields and decomposition products. The Krapcho protocol is based on the combined effect of a Lewis acid and water in highboiling, polar aprotic solvents like DMSO (dimethyl sulfoxide), under neutral conditions. In preliminary experiments performed at 100 °C, we did not detect the formation of the product ( Table  1, Entry 1). The increase of the reaction temperature at 130 °C led to the formation of the desired product 2. However, the optimized protocol depends also on the control of other two reaction parameters. In particular, at 0.10 molar concentration after 5 h of reaction time we observed about 60% conversion, determined by 1 H NMR on the crude, and 40% isolated yield of 2 (Entry 2). Increasing the reaction time at 18 h, we observed an almost complete disappearance of 1 and a good isolated yield (Entry 3). The reaction was also performed in a more concentrated media (0.20 M), giving similar results in a shorter reaction time (Entry 4). The difference between observed conversion and isolated yield is due in part to loss of product during the extraction with water in the work-up procedure for the removal of DMSO and in part because of some amount of decomposition products.

General Information
Reactions were performed using commercially available compounds without further purification and analytical grade solvents. All the reactions were monitored by thin layer chromatography (TLC) on precoated silica gel plates (0.25 mm) and visualized by fluorescence quenching at 254 nm. Flash chromatography was carried out using silica gel 60 (70-230 mesh, Merck, Darmstadt, Germany). The NMR spectra were recorded on Bruker (Rheinstetten, Germany) DRX 300 spectrometer (400 MHz, 1 H, 100 MHz, 13 C). Spectra were referenced to residual CHCl3 (7.26 ppm, 1 H, 77.00 ppm, 13 C). The following abbreviations are used to indicate the multiplicity in NMR spectra: s-singlet; d-doublet; m-multiplet; bs-broad signal. Coupling constants (J) are quoted in Hertz in NMR spectrum (see Supplementary Materials for 1 H NMR and 13 C NMR spectra). High resolution mass spectra (HRMS) were acquired using a Bruker solariX XR Fourier transform ion cyclotron resonance mass spectrometer (Bruker Daltonik GmbH, Bremen, Germany) equipped with a 7T refrigerated actively-shielded superconducting magnet. The samples were ionized in a positive ion mode using an electrospray (ESI) ionization source.

General Information
Reactions were performed using commercially available compounds without further purification and analytical grade solvents. All the reactions were monitored by thin layer chromatography (TLC) on precoated silica gel plates (0.25 mm) and visualized by fluorescence quenching at 254 nm. Flash chromatography was carried out using silica gel 60 (70-230 mesh, Merck, Darmstadt, Germany). The NMR spectra were recorded on Bruker (Rheinstetten, Germany) DRX 300 spectrometer (400 MHz, 1 H, 100 MHz, 13 C). Spectra were referenced to residual CHCl 3 (7.26 ppm, 1 H, 77.00 ppm, 13 C).
The following abbreviations are used to indicate the multiplicity in NMR spectra: s-singlet; d-doublet; m-multiplet; bs-broad signal. Coupling constants (J) are quoted in Hertz in NMR spectrum (see Supplementary Materials for 1 H NMR and 13 C NMR spectra). High resolution mass spectra (HRMS) were acquired using a Bruker solariX XR Fourier transform ion cyclotron resonance mass spectrometer (Bruker Daltonik GmbH, Bremen, Germany) equipped with a 7T refrigerated actively-shielded superconducting magnet. The samples were ionized in a positive ion mode using an electrospray (ESI) ionization source.

General Procedure for Synthesis and Characterization of 2
In a Schlenk tube to a solution of dimethyl 2-(1-methyl-3-oxoisoindolin-1-yl)malonate 1 (30 mg, 0.11 mmol, 1 eq.) in DMSO (500 µL) and water (50 µL) was added anhydrous lithium chloride (18 mg, 4 eq.). The reaction mixture was stirred at 130 • C till starting material disappeared by thin layer chromatography (CHCl 3 /AcOEt 1:4). The reaction mixture was diluted with ethyl acetate and washed with brine, then the organic phase was dried on anhydrous sodium sulphate and concentrated under reduced pressure to give an oil. Purification by flash chromatography on silica gel (Hexane/AcOEt 8:2) gave the pure product as a yellow waxe-type solid. Yield: 70% (24 mg). 1