2-(2-(4-Methoxyphenyl)-4,9-dimethyl-7-oxo-7 H -furo[2,3-f ]chromen-3-yl)acetic Acid

: For the ﬁrst time, we describe a new approach towards the synthesis of previously unknown 2-(2-(4-methoxyphenyl)-4,9-dimethyl-7-oxo-7 H -furo[2,3- f ]chromen-3-yl)acetic acid. The presented method is based on the multicomponent condensation of 5-hydroxy-4,7-dimethyl-2 H -chromen-2-one, 4-methoxyphenylglyoxal and Meldrum’s acid. It was shown that the studied reaction proceeds in two steps including the initial interaction of starting materials in MeCN and the ﬁnal formation of furylacetic acid moiety in acidic media. The structures of the obtained compound were established by 1 H, 13 C-NMR spectroscopy and high-resolution mass spectrometry.

In most cases, furocoumarins can be prepared on the basis of substituted hydroxycoumarins. α-Halogen ketones are generally employed as the second component for the formation of the furocoumarin moiety [23][24][25][26][27][28]. Wherein, the use of the methodology of multicomponent reactions can open access to a wide range of products containing the furocoumarin fragment. A significant advantage of this approach is the ability to obtain target products in one synthetic stage [29][30][31][32][33]. It should be noted that we previously proposed a general approach to the synthesis of condensed furylacetic acids based on the multicomponent reaction of various hydroxyl derivatives with arylglyoxals and Meldrum's acid [34][35][36][37][38]. We assumed that this approach could be used to synthesize substituted furo[2,3-f ]coumarins.

Results
In the present communication, we report that a multicomponent reaction of 5-hydroxy-4,7-dimethyl-2H-chromen-2-one 1, 4-methoxyphenylglyoxal 2 and Meldrum's acid 3 in the presence of Et 3 N leads to previously unknown 2-(2-(4-methoxyphenyl)-4,9-dimethyl-7oxo-7H-furo[2,3-f ]chromen-3-yl)acetic acid 4 (Scheme 1). Earlier, it was demonstrated that this type of reaction is a two-step cascade process. Herein, the interaction of components in acetonitrile (MeCN) proceeds at the first stage, and the final acid-catalyzed cyclization leads to the target product. It is important to note that in the considered case prolonged reflux (16 h) in MeCN is necessary for the synthesis of furocoumarin derivative 4. At the same time, it is necessary to use a 6-fold excess of arylglyoxal 2, Meldrum's acid 3, and Et 3 N for the complete conversion of coumarin 1 to target product 4. It should be noted that the starting compound 1 remains as an impurity in the resulting product 2 if a smaller excess of the above-mentioned reagents is used. Apparently, this difference is due to the low reactivity of the coumarin 1 compared with those of the previously studied hydroxyl derivatives. Wherein, a mixture of hydrochloric and acetic acids is used for the final cyclization similar to the previous works [34][35][36][37][38]. The presented method allows one to synthesize the target 2-(2-(4-methoxyphenyl)-4,9-dimethyl-7-oxo-7H-furo[2,3-f ]chromen-3-yl)acetic acid 4 with a 74% yield.
Molbank 2021, 2021, x FOR PEER REVIEW 4. At the same time, it is necessary to use a 6-fold excess of arylglyoxal 2, Meldru 3, and Et3N for the complete conversion of coumarin 1 to target product 4. It sh noted that the starting compound 1 remains as an impurity in the resulting prod smaller excess of the above-mentioned reagents is used. Apparently, this differen to the low reactivity of the coumarin 1 compared with those of the previously hydroxyl derivatives. Wherein, a mixture of hydrochloric and acetic acids is used final cyclization similar to the previous works [34][35][36][37][38]. The presented method all to synthesize the target 2-(2-(4-methoxyphenyl)-4,9-dimethyl-7-oxo-7H-f f]chromen-3-yl)acetic acid 4 with a 74% yield.
The proposed reaction mechanism is presented in Scheme 2. At the first ste action of Meldrum's acid 3 with arylglyoxal 2 leads to intermediate A. Next, the of coumarin anion B to Michael acceptor A results in the formation of adduct D. ther acid-catalyzed cleavage of Meldrum's acid moiety is followed by the elimin CO2 and acetone-produced γ-ketoacid F. Finally, intermediate F is transformed to get product 4 via cyclodehydration including the hydroxyl group of the couma ment and the carbonyl unit. In summary, a convenient one-pot cascade method for the synthesis of pr The proposed reaction mechanism is presented in Scheme 2. At the first step, interaction of Meldrum's acid 3 with arylglyoxal 2 leads to intermediate A. Next, the addition of coumarin anion B to Michael acceptor A results in the formation of adduct D. The further acid-catalyzed cleavage of Meldrum's acid moiety is followed by the elimination of CO 2 and acetone-produced γ-ketoacid F. Finally, intermediate F is transformed to the target product 4 via cyclodehydration including the hydroxyl group of the coumarin fragment and the carbonyl unit.
Molbank 2021, 2021, x FOR PEER REVIEW 2 of 5 4. At the same time, it is necessary to use a 6-fold excess of arylglyoxal 2, Meldrum's acid 3, and Et3N for the complete conversion of coumarin 1 to target product 4. It should be noted that the starting compound 1 remains as an impurity in the resulting product 2 if a smaller excess of the above-mentioned reagents is used. Apparently, this difference is due to the low reactivity of the coumarin 1 compared with those of the previously studied hydroxyl derivatives. Wherein, a mixture of hydrochloric and acetic acids is used for the final cyclization similar to the previous works [34][35][36][37][38]. The presented method allows one to synthesize the target 2-(2-(4-methoxyphenyl)-4,9-dimethyl-7-oxo-7H-furo[2,3f]chromen-3-yl)acetic acid 4 with a 74% yield.

Scheme 1. Synthesis of 2-(2-(4-methoxyphenyl)-4,9-dimethyl-7-oxo-7H-furo[2,3-f]chromen-3yl)acetic acid 4.
The proposed reaction mechanism is presented in Scheme 2. At the first step, interaction of Meldrum's acid 3 with arylglyoxal 2 leads to intermediate A. Next, the addition of coumarin anion B to Michael acceptor A results in the formation of adduct D. The further acid-catalyzed cleavage of Meldrum's acid moiety is followed by the elimination of CO2 and acetone-produced γ-ketoacid F. Finally, intermediate F is transformed to the target product 4 via cyclodehydration including the hydroxyl group of the coumarin fragment and the carbonyl unit. In summary, a convenient one-pot cascade method for the synthesis of previously unknown 2-(2-(4-methoxyphenyl)-4,9-dimethyl-7-oxo-7H-furo[2,3-f ]chromen-3-yl)acetic acid based on the multicomponent condensation of 5-hydroxy-4,7-dimethyl-2H-chromen-2one, 4-methoxyphenylglyoxal and Meldrum's acid was elaborated. The advantages of this approach are the application of readily available starting compounds, atom economy, and easy work-up procedures, which can avoid chromatographic purification. The structure of the synthesized furocoumarin was confirmed by 1 H, 13 C-NMR spectroscopy and highresolution mass spectrometry.

Materials and Methods
All starting chemicals and solvents were commercially available and were used as received. NMR spectra were recorded with Bruker DRX 500 (500 MHz) spectrometers (Billerica, MA, USA) in DMSO-d 6 . Chemical shifts (ppm) were given relative to solvent signals (DMSO-d 6 : 2.50 ppm ( 1 H NMR) and 39.52 ppm ( 13 C NMR)). High-resolution mass spectra (HRMS) were obtained on a Bruker micrOTOF II instrument (Bruker Daltonik Gmbh, Bremen, Germany) using electrospray ionization (ESI). The melting points were determined on a Kofler hot stage (Dresden, Germany). IR spectra were recorded on a Bruker ALPHA (Santa Barbara, CA 93117, USA) spectrophotometer in a KBr pellet.