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Diastereoselective Formal Synthesis of a Monoterpene Alkaloid, (-)-Incarvilline

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Diastereoselective Formal Synthesis of a Monoterpene Alkaloid, (-)-Incarvilline Diastereoselective Formal Synthesis of a Monoterpene Alkaloid, (-)-Incarvilline Toshio Honda* and Kyosuke Kaneda Faculty of Pharmaceutical Sciences, Hoshi UniVersity, Ebara 2-4-41, Shinagawa-ku, Tokyo 142-8501, Japan honda@hoshi.ac.jp ReceiVed May 9, 2007 Diastereoselective formal synthesis of a monoterpene alkaloid, (-)-incarvilline, the key intermediate for the synthesis of (-)-incarvillateine, was achieved by using an intramolecular Pauson-Khand reaction of (S)-N-[(E)-2-butenyl]-N-(3-butynyl-2-methoxymethoxy)-p-toluenesulfonamide as a key step. Introduction To the best our knowledge, two total syntheses4,6 and one synthetic approach7 for 3 have been reported to date. Recent investigations of the plant IncarVilla sinensis,1 which As part of our continuing effort to synthesize biologically has been used to treat rheumatism and relieve pain as a active natural products, we are also interested in a diastereo- traditional Chinese medicine, led to the isolation of a various selective synthesis of (-)-incarvilline. Our retrosynthetic analy- types of monoterpene alkaloids with a wide range of structural sis was depicted in Scheme 1, where we decided to exploit an and stereochemical features. Among them, incarvillateine 1 intramolecular Pauson-Khand reaction8 of (S)-N-[(E)-2-bute- carrying a characteristic cyclobutane ring has been recognized nyl]-N-(3-butynyl-2-methoxymethoxy)-p-toluenesulfonamide as to exhibit significant antinociceptive activity in a formalin- a key step, since the relative stereochemistry between the 7- induced pain model in mice.2 It is also suggested that the and 7a-positions should be controlled by employing E-olefin antinociceptive effect arose from the activation of µ- and as the starting material. The desired absolute configuration at κ-opioid receptors and adenosine receptor3 (Figure 1). the 7a-position should also be constructed, stereoselectively, with Incarvillateine 1 was supposed to generate biosynthetically reflecting stereochemistry at the 4-position by assuming steric - via dimerization of incarvine C 2, a hydroxycinnamate derivative repulsion between the propargylic substituent and dicobalt of a monoterpene alkaloid, incarvilline 3. In fact, the first total alkyne carbonyl complex generated in the intermediate of this synthesis of incarvillateine 1 using photochemical dimerization (5) (a) Chi, Y.-M.; Yan, W.-M.; Chen, D.-C.; Noguchi, H.; Iitaka, Y.; of a hydroxycinnamic acid derivative, followed by esterification Sankawa, U. Phytochemistry 1992, 31, 2930-2932. (b) Chi, Y.-M.; + Hashimoto, F.; Yan, W.-M.; Nohara, T.; Yamashita, M.; Marubayashi, N. with ( )-6-epi-incarvilline, was achieved by Kibayashi and co- Chem. Pharm. Bull. 1997, 45, 495-498. workers.4 (6) Ichikawa, M.; Aoyagi, S.; Kibayashi, C. Tetrahedron Lett. 2005, 46, - Thus, development of a new synthetic strategy for incarvilline 2327 2329. 5 (7) Hong, B.-C.; Gupta, A. K.; Wu, M.-F.; Liao, J.-H.; Lee. G.-H. Org. 3 would be an important research subject directed at searching Lett. 2003, 5, 1689-1692. potential antinociceptive compounds related to incarvillateine. (8) (a) Khand, I. U.; Knox, G. R.; Pauson, P. L.; Watts, W. E. J. Chem. Soc., Chem. Commun. 1971, 36. (b) Khand, I. U.; Knox, G. R.; Pauson, P. L.; Watts, W. E.; Foreman, M. I. J. Chem. Soc., Perkin Trans. 1 1973, * Corresponding author. Tel: +81 (0)3 5498 5791. Fax: +81 (0)3 3787 0036. 977-981. (c) Exon, C.; Magnus, P. J. Am. Chem. Soc. 1983, 105, 2477- (1) Chi, Y.; Yan, W.-M.; Li, J.-S. Phytochemistry 1990, 29, 2376-2378. 2478. (d) Magnus, P.; Principe, L. M. Tetrahedron Lett. 1985, 26, 4851- (2) Nakamura, M.; Chi, Y.-M.; Yan, W.-M.; Nakasugi, Y.; Yoshizawa, 4854. For recent reviews, see also: (e) Schore, N. E. Org. React. 1991, 40, T.; Irino, N.; Hashimoto, F.; Kinjo, J.; Nohara, T.; Sakurada, S. J. Nat. 1-90. (f) Fru¨hauf, H.-W. Chem. ReV. 1997, 97, 523-596. (g) Geis, O.; Prod. 1999, 62, 1293-1294. Schmalz, H.-G. Angew. Chem., Int. Ed. 1998, 37, 911-914. (h) Brummond, (3) Chi, Y.; Nakamura, M.; Yoshizawa, T.; Zhao, X-Y.; Yan, W.-M.; K. M.; Kent, J. L. Tetrahedron 2000, 56, 3263-3283. (i) Fletcher, A. J.; Hashimoto, F.; Kinjo, J.; Nohara, T.; Sakurada, S. Biol. Pharm. Bull. 2005, Christie, S. D. R. J. Chem. Soc., Perkin Trans. 1 2000, 1657-1668. (j) 28, 1989-1991. Blanco-Urgoiti, J.; Anorbe, L.; Perez-Serrano, L.; Dominguez, G.; Perez- (4) Ichikawa, M.; Takahashi, M.; Aoyagi, S.; Kibayashi, C. J. Am. Chem. Castells, J. Chem. Soc. ReV. 2004, 33,32-42. (k) Bon˜aga, L. V. R.; Krafft, Soc. 2004, 126, 16553-16558. M. E. Tetrahedron 2004, 60, 9795-9833. 10.1021/jo0709091 CCC: $37.00 © 2007 American Chemical Society Published on Web 07/21/2007 J. Org. Chem. 2007, 72, 6541-6547 6541 Honda and Kaneda FIGURE 1. 1. Structure of typical alkaloids in IncarVillea sinensis. SCHEME 1. Retrosynthetic Analysis for 3 FIGURE 2. 2. Structure determination of 14 and 15 (observed NOEs are indicated by arrows). SCHEME 2. Attempted Preparation of the Precursor for Pauson-Khand Reaction FIGURE 3. 3. Intermediates for Pauson-Khand reaction. FIGURE 4. 4. Structure determination of 23 and 24 (observed NOEs are indicated by arrows). reaction. Similar diastereoselectivity for an intramolecular - Pauson Khand reaction of enynes having a substituent at the Results and Discussion propargylic position to construct a bicyclic cylopentenone system has been observed in previous works.9 Moreover, it has Given these considerations, our synthesis of a monoterpene been known that the methyl group at the 4-position could be alkaloid, (-)-incarvilline, commenced with the synthesis of the derived from the corresponding alkene by catalytic reduction,4 known (S)-4-tert-butyldimethylsiloxy-1-butyn-3-ol 5,11 which which could be available from the ketone as a precursor (Scheme was readily accessible via the known (S)-1-butyne-3,4-diol 4 1). It is noteworthy that Schore and his colleauges reported a from D-(-)-mannitol. Methoxymethylation of (S)-4-tert-bu- similar methodology in the synthesis of racemic tecomanine,10 tyldimethylsiloxy-1-butyn-3-ol 5 with chloromethyl methyl ether where they isolated the cycloaddition products in up to 16% afforded methoxymethyl ether 6 in good yield. Desilylation of yield with diastereoselectivity opposite to our assumption and 6 with tetrabutylammonium fluoride gave alcohol 7 in 91% also to the results of the previous works.9 yield. Introduction of butenylamino group was first attempted by (9) (a) Jeong, N.; Lee, B. Y.; Lee, S. M.; Chung, Y. K.; Lee, S.-G. treatment of 7 with N-(2E)-2-butenyl-p-toluenesulfonamide - Tetrahedron Lett. 1993, 34, 4023 4026. (b) Clive, D. L. J.; Cole, D. C.; under the Mitsunobu reaction conditions.12 However, none of Tao, Y. J. Org. Chem. 1994, 59, 1396-1406. (c) Krafft, M. E.; Chirico, X. Tetrahedron Lett. 1994, 35, 4511-4514. (d) Mukai, C.; Uchiyama, M.; the desired product 10 could be isolated, unfortunately. Although Sakamoto, S.; Hanaoka, M. Tetrahedron Lett. 1995, 36, 5761-5764. (e) reaction of 7 with N-(tert-butoxycarbonyl)-p-toluenesulfonamide Mukai, C.; Kim, J. S.; Uchiyama, M.; Hanaoka, M. Tetrahedron Lett. 1998, gave the desired tosylamide 8, subsequent deprotection of the 39, 7909-7912. (f) Gu¨nter, M.; Gais, H.-J. J. Org. Chem. 2003, 68, 8037- 8041. (g) Mukai, C.; Kozuka, T.; Suzuki, Y.; Kim, I. J. Tetrahedron 2004, 60, 2497-2507. (h) Nomura, I.; Mukai, C. J. Org. Chem. 2004, 69, 1803- (11) Gooding, O. W.; Beard, C. C.; Jackson, D. Y.; Wren, D. L.; Cooper, 1812. G. F. J. Org. Chem. 1991, 56, 1083-1088. (10) Ockey, D. A.; Lewis, M. A.; Schore, N. E. Tetrahedron 2003, 59, (12) (a) Mitsunobu, O. Synthesis 1981,1-28. (b) Tsunoda, T.; Yamamiya, 5377-5381. Y.; Ito, S. Tetrahedron Lett. 1993, 34, 1639-1642. 6542 J. Org. Chem., Vol. 72, No. 17, 2007 Synthesis of a Monoterpene Alkaloid, (-)-IncarVilline SCHEME 3. Preparation of the Precursor 10 for Pauson-Khand Reaction TABLE 1. Pauson-Khand Reaction of 10 SCHEME 4. Preparation and Attempted Pauson-Khand Reaction of 16 (NMO)14 under argon, the reaction was found to proceed at ambient temperature; however, the yield was decreased to 50% yield (%) with a formation of 14/15 in a ratio of 9:1 (entry 2). 15 entry promoter (equiv) solvent atm T (°C) time (h) 14 15 By changing a promoter to butyl methyl sulfides, a similar reaction was carried out in refluxing dichloroethane (DCE) under 1 none toluene Ar 110 2 54 7 argon to give 14 in slightly better yield (entries 3 and 5). The 2 NMO (10) CH2Cl2 Ar rt 9 45 5 3 n-BuSMe (3.5) DCE Ar 83 24 58 7 best result was obtained when the reaction was carried out by 4 n-BuSMe (3.5) DCE CO 83 2.5 66 7 employing 1.05 equiv of Co2(CO)8 in refluxing DCE in the 5 t-BuSMe (3.5) DCE Ar 83 2.5 62 6 presence of 3.5 equiv of tert-butyl methyl sulfide as the promoter 6 t-BuSMe (3.5) DCE CO 83 2.5 73 8 for 2.5 h under an atmosphere of CO to give 14 in 73% yield together with 15 in 8% yield (entry 6). Boc group did not provide the corresponding amide 9 under The diastereoselectivity can be rationalized by assuming that various reaction conditions (Scheme 2). the cyclization would proceed through the sterically favored For preparation of the requisite enyne amide 10, alcohol 7 intermediate (A) leading to 14, rather than the intermediate (B), was converted to tosylate 11 in 91% yield. Treatment of 11 in which the steric repulsion between MOM and dicobalt with sodium azide in DMSO gave azide 12, which without complex moieties was observed, as shown in Figure 3.
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