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Ghorai, Sujit Kumar; De, Saroj Ranjan; Karmakar, Raju; Hazra, Nirmal Kumar; Mal, Dipakranjan

doi:https://doi.org/10.1155/2009/528081

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Abstract Introduction Results and Discussion Conclusion Experimental Acknowledgments References Copyright Related Articles

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Volume 2009 | Article ID 528081 | https://doi.org/10.1155/2009/528081

Synthesis of Benzo[]fluorenone Nuclei of Stealthins

Sujit Kumar Ghorai,¹Saroj Ranjan De,¹Raju Karmakar,¹Nirmal Kumar Hazra,¹and Dipakranjan Mal¹

Academic Editor: Robert Strongin

Received03 Dec 2008

Accepted16 Feb 2009

Published24 Mar 2009

Abstract

Two routes, one based on a Michael-initiated aldol condensation and the other on an intramoleculer carbonyl-ene reaction, have been found to be feasible for an entry to benzo[]fluorenones. Reaction of 4,9-dimethoxybenz[]indenone with nitromethane in the presence of DBU gave the corresponding Michael adduct, which afforded 2-methyl-5,10-dimethoxybenzo[b]fluorenone on reaction with methacrolein under a variety of basic conditions. Similarly, 2-methallyl-4,9-dimethoxybenz[]indenone reacted with nitromethane to give the corresponding Michael adduct, Nef reaction of which furnished 3-formyl-2-methyl-4,9-dimethoxybenz[]indanone. This underwent ene-cyclization under the influence of SnCl4. 5H2O, and yielded 2-methyl-5,10-dimethoxybenzo[]fluorenone.

1. Introduction

Stealthins A (1a) and B (1b), isolated from Streptomyces viridochromogenes as potent radical scavengers, are the first known members of natural benzofluorenones [1]. Interest in this group of compounds grew considerably due to the identification of structurally allied natural products, stealthin C (1c) [2], kinafluorenone (2) [3], prekinamycin (3) [4], and kinamycin antibiotics (e.g., kinamycin D, 4) [5] (Figure 1). Their synthesis became an active area of research since 1996 [6–19]. In line with the Ishikawa approach [19], we intended to explore the chemistry of benzindenones (e.g., 5b) to establish new synthetic routes to functionalized benzofluorenones [20]. Herein, we report regiospecific construction of the D-ring of benzofluorenones (e.g., 6) from the corresponding benzindenones.

2. Results and Discussion

Initial studies were focused on the utilization of the readily accessible benzindenones 5a and 5b [21]. DBU-promoted Michael addition of nitromethane to the indenones furnished indenones 7a and 7b, respectively. The intended annulation of 7b with methacrolein was then studied with different base-solvent systems (Scheme 1). But, none of the attempts gave desired product 8. Instead, most of the methods produced benzofluorenone 6 in low yields. The best yield was 25%, which was obtained with DBU in benzene. The presence of singlet at δ 2.23 for Ar-C in NMR spectrum was indicative of the structure 6. It is probable that the compound 6 was formed from tetracycle 8 through elimination of HN. Considering the fact that even a weak base such as -BP caused the elimination of N group, we examined the route (Scheme 2), involving an acid-catalyzed cyclization. The Synthon equivalent 9 was prepared in two steps from methacrolein by adaptation of Miyakoshi protocol [22] (Scheme 2). Conjugate addition of the reagent 9 to benzindenone 5b in the presence of DBU provided 10 in good yield. NMR spectrum of the product indicated the formation of a 1:1 mixture of diastereomers. When treated with 1 N HCl, the mixture afforded the expected product 8 in trace amount, the major product being 6 (25%). Repeated attempts to optimize the transformation of 10 into 8 were of no avail.

As an alternative avenue, the strategy (Scheme 3) based upon the intramolecular carbonyl-ene reaction [23] of 11 was undertaken. Preparation of the key precursor 11 is depicted in Scheme 3. LDA-promoted allylation of 12 [21] with allyl bromide 13a furnished 14a. Characteristic multiplets at δ 5.6 and two doublets at δ 5.1 and δ 4.87 in NMR spectrum were in complete agreement with the structure 14a. The cis-relationship between the angular allyl group and the methano bridge was inferred by comparing the NMR signals of C-4a H of an angularly methylated analog [24]. Flash vacuum pyrolysis (FVP) of the adduct 14a at C/0.01 mm gave enone 5c in sufficiently pure form for the next use. It was then subjected to conjugate addition with nitromethane in the presence of DBU to produce allylated nitro adduct 15a as a single isomer in 92% yield (Scheme 3). Similarly, precursor 15b was obtained in three steps from 12. Methallylation of 12 with methallyl iodide 13b in the presence of LDA gave 14b (91%), FVP of which furnished 5d. Addition of nitromethane to 5d in the presence of DBU-furnished intermediate 15b in 80% yield. Nef reaction [25] of 15b with NaOMe and TiC-buffer provided aldehyde 11 in moderate yield (50%). The singlet at δ 9.94 in NMR spectrum and the band at 1718 in IR spectrum confirmed the presence of CHO functionality in 11. When a solution of the aldehyde in dichloromethane was treated with SnC 5O [26], D-ring aromatized compound 6 was formed in 45% yield.

3. Conclusion

We have validated two synthetic routes to benzofluoren-11-ones from benzindenones 5. The intramolecular carbonyl-ene reaction of the intermediate 11 (Scheme 3) proved to be better pathway than the tandem Michael-aldol route (Scheme 2) to benzofluoren-11-one 6.

4. Experimental

The general experimental is described in [27].

Benzinden-1-One 5c
This compound was prepared from 14a. Mp: 80–85; yellow; yield 93%; IR (): 1684; NMR (200 MHz), 8.20 (d, 1H, J = 8.1), 7.97 (d, 1H, J = 8.1), (m, 3H), (m, 1H), (m, 2H), 4.28 (s, 3H), 4.02 (s, 3H), (m, 2H); NMR (50 MHz): 193.99, 152.2, 144.6, 141.5, 139.8, 134.5, 132.9, 131.1, 129.4, 127.1, 126.2, 125.7, 123.0, 117.1, 115.5, 62.8, 62.7, 29.5; MS (m/z): 280 (M+, 100%), 265, 250, 223, 178, 165.

Benzinden-1-One 5d
This compound was prepared as a yellow oil in 90% yield from 14b. IR (): 1689; NMR (300 MHz): 8.10 (d, 1H, J = 8.1), 7.97 (d, 1H, J = 8.1), (m, 3H), 4.85 (d, 2H, J = 10.8), 4.28 (s, 3H), 4.02 (s, 3H), 3.04 (s, 2H), 1.79 (s, 3H); NMR (75 MHz): 192.9, 152.0, 144.5, 142.6, 140.9, 140.4, 132.7, 131.0, 129.3, 127.0, 126.0, 125.6, 122.9, 115.3, 112.5, 62.9, 62.7, 33.3, 22.5; MS (m/z): 294 (M+, 100%), 279, 263, 236, 165, 152, 139.

Benzofluorenone 6: Method A
To a stirred solution of the nitro compound 7a (100 mg, 0.33 mmol), and methacrolein (60 mg, 0.86 mmol) in benzene (5 mL) at 0 was added DBU (10 mg, 0.066 mmol). Stirring was continued for 24 hours at rt. The reaction mixture was diluted with diethyl ether (50 mL), washed with saturated sodium bicarbonate solution (10 mL) and then with brine (10 mL). The organic phase was dried (NS) and concentrated. The resulting residue was purified by preparative TLC to give a yellow crystalline solid of 6 (26 mg, 25%).

Method B
To a stirred solution of aldehyde 11 (50 mg, 0.154 mmol) in dichloromethane (6 mL) was added SnC O (5 mg) under nitrogen atmosphere. The stirring was continued for 30 hours. After usual work up of the reaction mixture, the residue was purified by preparative TLC to provide 6 (21 mg, 45%). Mp: 150-151; IR (): 1695; NMR (200 MHz): 8.29 (d, 1H, J = 7.4), 8.04 (d, 1H, J = 7.4), 7.88 (d, 1H, J = 7.7), (m, 4H), 4.28 (s, 3H), 4.00 (s, 3H), 2.42 (s, 3H); NMR (50 MHz): 190.4, 153.7, 146.4, 140.0, 138.8, 136.4, 135.4, 133.6, 130.8, 129.4, 127.8, 126.7, 125.5, 124.4, 124.1, 122.4, 119.9, 63.1, 61.1, 21.3; MS (m/z): 304 (M+, 100%), 289, 218, 189, 149, 57.

Compound 7a
This was prepared from benzindenone 5a and nitromethane in 89% yield according to the procedure described earlier [25]. Mp: 124; IR (): 1711; NMR (200 MHz): 8.37 (s, 1H, ArH) 8.03 (d, 1H, J = 8.1), (m, 2H), (m, 2H), (ABq, 1H, J = 12.8, 5.8), (ABq, 1H, J = 12.8, 5.8), (m, 1H), (ABq, 1H, J = 19.2, 8.2), (ABq, 1H, J = 19.2, 3.9).

Compound 7b
This was prepared from 5b, following the procedure described for compound 7a. Mp: 179-180; white solid; yield: 89%; IR (): 1715; NMR (200 MHz): 8.40 (d, 1H, J = 8.2), 8.10 (d, 1H, J = 8.5), (m, 2H), (m, 1H), (m, 2H), 4.18 (s, 3H), 4.03 (s, 3H) (m, 1H), (m, 1H); NMR (50 MHz): 200.4, 152.9, 148.6, 134.1, 132.7, 129.7, 126.9, 125.3, 122.7, 121.8, 77.8, 77.2, 63.4, 61.8, 42.3, 34.4; MS (m/z): 301 (M+), 254, 239, 197, 141, 115.

Compound 8
To a mixture of enone 5b (0.178 g, 0.740 mmol) and 1,1-ethanediyldioxy-2-methyl-4-nitrobutane 9 (0.389 g, 2.22 mmol) in CC (4 mL) was added DBU (12 mg, 0.078 mmol) and the mixture was stirred at rt for 6 hours. It was then concentrated and purified by column chromatography to afford 10 as an oil (0.2 g, 65%). NMR spectrum revealed the presence of two isomers as indicated by three signals δ 4.15, 4.08, and 4.05, corresponding to the methoxy groups. The peak at δ 4.15 was not resolved. The methine hydrogens of CHN appeared at δ 5.19. To a stirred solution of above nitro acetal 10 (100 mg, 0.24 mmol) in THF (8 mL) was added 10% HCl (1 mL) solution. Stirring was continued for 20 hours. After usual work up of the reaction mixture, the residue was chromatographed to afford 6 (18 mg, 25%) and 8 (2.5 mg, 3%).

Compound 9
Yield: 50%; colorless oil; IR (): 1541; NMR (200 MHz): 4.66 (d, 1H, J = 4), 4.46 (t, 2H, J = 6), (m, 4H), (m, 3H), 1.00 (d, 3H, J = 6.7); NMR (50 MHz): 106.8, 74.1, 65.1, 65.0, 34.3, 29.0, 14.7.

Compound 11
This was prepared from compound 15b by Nef reaction [25]. Yield: 50%; purity > 80%; NMR (500 MHz): 9.94 (s, 1H), 8.40 (d, 1H, J = 8.4), 8.10 (d, 1H, J = 8.4), 7.69 (t, 1H, J = 8.2), 7.52 (t, 1H, J = 8.2), 4.87 (s, 1H), 4.78 (s, 2H), 4.21 (s, 3H), 4.16 (brs, 1H), 4.02 (s, 3H) (m, 1H); (ABq, 1H, J = 14.0, 4.3) 1.75 (s, 3H).

Compound 12
NMR (200 MHz): 8.37 (d, 1H, J = 8.0, 1H), 8.05 (d, 1H, J = 8.0, 1H), (m, 2H), 6.85 (brs, 1 H), (m, 1H), 4.32 (s, 3H), 3.70 (s, 3H), 2.85 (brs, 1H), (m, 1H), (m, 2H), (m, 3H).

Compound 14a
This was prepared as thick brownish oil in 88% yield from pentacycle 12, following an earlier method [24]. IR (): 1705; NMR (300 MHz): 8.33 (d, 1H, J = 8.7), 8.06 (d, 1H, J = 8.4), 7.61 (m, 1H), 7.49 (m, 1H), (m, 1H), (m, 2H), 5.07 (d, 1H, J = 16.8), 4.85 (d, 1H, J = 10.2), 4.08 (s, 3H), 4.03 (s, 3H), 3.78 (d, 1H, J = 4.2), 3.45 (brs, 1H), (m, 2H), (m, 1H), 2.0 (ABd, 1H, J = 8.7), 1.80 (ABd, 1H, J = 8.7); NMR (75 MHz): 207.1, 151.2, 147.6, 138.0, 135.2, 135.1, 134.3, 132.4, 128.9, 126.6, 125.8, 125.0, 121.8, 117.5, 63.0, 62.4, 62.1, 50.8, 50.9, 47.0, 46.6, 41.6.

Compound 14b
This was prepared from pentacycle 12, following the procedure adopted for compound 14a. Yield: 89%; thick oil; IR (): 1705; NMR (400 MHz): 8.32 (d, 1H, J = 8.1), 8.07 (d, 1H, J = 8.1), 7.62 (br t, 1H), 7.49 (br t, 1H), 6.00 (dd, 1H, J = 2.8, 5.6), 5.49 (dd, 1H, J = 2.8, 5.6), 4.70 (brs, 1H), 4.66 (brs, 1H), 4.08 (s, 3H), 4.03 (s, 3H), 3.93 (d, 1H, J = 4), 3.44 (brs, 1H), 3.05 (ABd, 1H, J = 13.8), 2.94 (brs, 1H), 2.41 (ABd, 1H, J = 13.8), 1.98 (ABd, 1H, J = 8.8), 1.79 (ABd, 1H, J = 8.8), 1.46 (s, 3H); NMR (50 MHz): 207.4, 151.0, 147.6, 143.1, 138.3, 135.5, 135.3, 134.6, 132.3, 128.8, 126.7, 125.8, 125.0, 121.8, 114.3, 62.8, 61.8, 61.6, 52.5, 50.8, 46.8, 46.1, 45.7, 23.8.

Compound 15a
This was prepared from 5c, following the procedure described for compound 7a. Mp: 98-99; white solid; yield: 92%; IR (): 1712; NMR (300 MHz): 8.40 (d, 1H, J = 8.7), 8.10 (d, 1H, J = 8.4), (m, 1H), 7.58 (m, 1H), (m, 1H), (m, 3H), (m, 1H), 4.20 (s, 3H), 4.10 4.05 (m, 1H), 4.01 (s, 3H), (m, 1H); (m, 2H); NMR (75 MHz): 202.7, 153.1, 148.7, 133.8, 133.3, 133.0, 129.8, 127.0, 125.4, 122.3, 121.9, 118.8, 77.7, 77.3, 63.4, 61.8, 52.2, 39.4, 36.1; MS (m/z): 341 (M+), 307, 290, 280 (100%), 265, 165.

Compound 15b
This was prepared from 5d, following the procedure adopted for compound 7a. Mp: 122-123; white solid; yield: 90%; IR (): 1707; NMR (300 MHz): 8.41 (d, 1H, J = 8.4), 8.10 (d, 1H, J = 8.4), (m, 1H), (m, 1H), 5.07 (dd, 1H, J = 12.8, 4.2), 4.88 (s, 1H), 4.76 (s, 1H), 4.59 (dd, 1H, J = 12.8, 8.7), 4.20 (s, 3H), (m, 1H), 4.00 (s, 3H), (m, 1H); 2.63 (dd, 1H, J = 13.8, 5.1), 2.34 (dd, 1H, J = 13.8, 9.0), 1.73 (s, 3H); NMR (75 MHz): 202.8, 153.3, 148.8, 142.5, 133.3, 132.9, 129.9, 129.8, 126.9, 125.3, 122.0, 114.2, 77.8, 63.3, 61.9, 50.8, 40.5, 39.9, 21.9. MS (m/z): 355 (M+), 319, 304, 294 (100%), 279, 265, 253, 236, 223, 165, 152, 139; anal. calcd for N: C, 67.59; H, 5.96; N, 3.94, found C, 67.51; H, 5.93; N, 3.93.

Acknowledgments

This work was supported by the Council of Scientific and Industrial Research (CSIR) and the Department of Science and Technology, New Delhi. The second and the third authors are grateful to the CSIR, for their research fellowships.

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Copyright © 2009 Sujit Kumar Ghorai et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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