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Synthesis 2020; 52(22): 3420-3426
DOI: 10.1055/s-0040-1707279
DOI: 10.1055/s-0040-1707279
special topic
Synthesis in Industry
Synthesis of an Azabicyclo[3.1.0]hexanone-Containing Inhibitor of NF-κΒ Inducing Kinase via Catalytic C–H Activation
This work was supported by Genentech (a member of the Roche group).
Abstract
The synthesis of an azabicyclo[3.1.0]hexanone-containing inhibitor of the nuclear factor-κB inducing kinase (NIK) is reported. The initial route to this compound was streamlined from 13 to 7 linear steps through the use of a catalytic, enantioselective C–H activation step. A procedure for lactam oxidation was identified that avoided use of peroxides on scale. These synthetic improvements allowed for the synthesis of multigram quantities of the desired NIK inhibitor for in vivo profiling.
Key words
C–H activation - NIK inhibitor - enantioselective - azabicyclo-[3.1.0]hexanone - nuclear factor-κB - medicinal chemistrySupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0040-1707279.
- Supporting Information
Publication History
Received: 28 July 2020
Accepted: 12 August 2020
Article published online:
15 September 2020
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References
- 1 Brightbill HD, Suto E, Blaquiere N, Ramamoorthi N, Sujatha-Bhaskar S, Gogol EB, Castanedo GM, Jackson BT, Kwon YC, Haller S, Lesch J, Bents K, Everett C, Kohli PB, Linge S, Christian L, Barrett K, Jaochico A, Berezhkovskiy LM, Fan PW, Modrusan Z, Veliz K, Townsend MJ, Devoss J, Johnson AR, Godemann R, Lee WP, Austin CD, McKenzie BS, Hackney JA, Crawford JJ, Staben ST, Ismaili MH. A, Wu LC, Ghilardi N. Nat. Commun. 2018; 9: 179
- 2 Sun S.-C. Nat. Rev. Immunol. 2017; 17: 545
- 3 Hofmann J, Mair F, Greter M, Schmidt-Supprian M, Becher B. J. Exp. Med. 2011; 208: 1917
- 4 Liao G, Zhang M, Harhaj EW, Sun S.-C. J. Biol. Chem. 2004; 279: 26243
- 5 Sun S.-C. Cell Res. 2011; 21: 71
- 6 Senftleben U, Cao Y, Xiao G, Greten FR, Krähn G, Bonizzi G, Chen Y, Hu Y, Fong A, Sun S.-C, Karin M. Science 2001; 293: 1495
- 7 Castanedo G, Liu Y, Crawford JJ, Braun M.-G. J. Org. Chem. 2016; 81: 8617
- 8 Li Z, Li X, Su M.-B, Gao L.-X, Zhou Y.-B, Yuan B, Lyu X, Yan Z, Hu C, Zhang H, Luo C, Chen Z, Li J, Zhao Y. J. Med. Chem. 2020; 63: 4388
- 9 Blaquiere N, Castanedo GM, Burch JD, Berezhkovskiy LM, Brightbill H, Brown S, Chan C, Chiang P.-C, Crawford JJ, Dong T, Fan P, Feng J, Ghilardi N, Godemann R, Gogol E, Grabbe A, Hole AJ, Hu B, Hymowitz SG, Ismaili MH. A, Le H, Lee P, Lee W, Lin X, Liu N, McEwan PA, McKenzie B, Silvestre HL, Suto E, Sujatha-Bhaskar S, Wu G, Wu LC, Zhang Y, Zhang Z, Staben ST. J. Med. Chem. 2018; 61: 6801
- 10 Blaquiere N, Burch J, Castanedo G, Feng JA, Hu B, Staben S, Wu G, Yuen P.-w. PCT Int. Appl WO 2015/025025 A1, 2015
- 11 Blaquiere N, Castanedo G, Feng JA, Crawford JJ, Lee W, Lin X, Hu B, Wu G. PCT Int. Appl WO 2016/135163 A1, 2016
- 12 Crawford JJ, Kolesnikov A, Feng JA. PCT Int. Appl WO 2018/037059 A1, 2018
- 13 Camici L, Dembech P, Ricci A, Seconi G, Taddei M. Tetrahedron 1988; 44: 4197
- 14 Hamann LG, Khanna A, Kirby MS, Magnin DR, Simpkins LM, Sutton JC, Robl J. PCT Int. Appl WO 2005/012249 A2, 2005
- 15 Dembech P, Ricci A, Seconi G, Taddei M. Org. Synth. 1997; 74: 84
- 16 Pedroni J, Cramer N. Angew. Chem. Int. Ed. 2015; 54: 11826
- 17 Zhang S.-Y, Li Q, He G, Nack WA, Chen G. J. Am. Chem. Soc. 2013; 135: 12135
- 18 Jerhaoui S, Chahdoura F, Rose C, Djukic J.-P, Wencel-Delord J, Colobert F. Chem. Eur. J. 2016; 22: 17397
- 19 Minami T, Fukuda K, Hoshiya N, Fukuda H, Watanabe M, Shuto S. Org. Lett. 2019; 21: 656
- 20a Caro-Diaz EJ. E, Urbano M, Buzard DJ, Jones RM. Biorg. Med. Chem. Lett. 2016; 26: 5378
- 20b He J, Wasa M, Chan KS. L, Shao Q, Yu J.-Q. Chem. Rev. 2017; 117: 8754
- 21a Meyers AI, Sturgess MA. Tetrahedron Lett. 1988; 29: 5339
- 21b Forns P, Fernández M, Diez A, Rubiralta M, Cherrier MP, Bonin M, Quirion J.-C. Synthesis 1999; 258
- 22 Sieber JD, Morken JP. J. Am. Chem. Soc. 2008; 130: 4978