tamiflu - university of texas at austingbdong.cm.utexas.edu/seminar/old/tamiflu_hee nam.pdf ·...
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http://commons.wikimedia.org/wiki/File:Tamiflu_75mg_german_closeup.jpg
Tamiflu: still needs
total synthesis?Group MeetingLiterature Talk12-19-2013Hee Nam LimProf. Guangbin Dong Group
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http://kansasheart.com/2012/09/tis-the-seasonits-time-for-your-flu-shot/
In 1918 Influenza in Spain (H1N1) pandemicInfected 500 million peoplekilled 50-100 million people
In 1957 and 1968 Asian flu (H2N2)Killed about 70,000 people
In 1997, Hongkong Avian flu (H5N1)Infected over 100 people, half died.
Kills 20,000 – 40,000 AmericansUS Healthcare - $12 billion dollors
New viruses are being reported (e.g. H7N9, Swine influenza…)
http://www.flu.gov/pandemic/history/
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- First developed by Gilead Sciences in 1995 and commercialized by F. Hoffman-La Loche Ltd in 1999. - The patent will be expired in 2016.
Oseltamivir (TamifluTM)- Treatment for Influenza A and B virus- Neuroaminidase Inhibitor: reduce symptoms and prevents the spread and infection to other cells.- Effective to H5N1 (AI) and H1N1 viruses
CO2EtO
AcHN
NH2 H3PO4
O CO2H
AcHNHN
NH
NH2
HO
OH
Zanamivir (RelenzaTM)
Limitation:Must be administered by inhalation
Javier Magano Tetrahedron 2011, 67, 7875-7889.
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Stats. for Tamiflu Research
“Oseltamivir” - 4850 hit in SCI Finder
0
100
200
300
400
500
600
700
800
900
No. of reports
About 60 research papersrelated to the synthesis of Oseltamivir have been published.(total synthesis, modification,formal synthesis)
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What’s good? - Proactive drug, water soluble -> orally available- Still best drug in the treatment of influenza viruses- Mildness -> allow administration to infants <1 year
What are issues?- Side effects (nausea, vomiting, diarrhea, abdominal pain, and headache, etc..)- Production shortage - limited source of starting material(dose – twice a day/ 75 mg, every year, 400 million packs are produced)- Mutants resistant to the current drug- No other effective alternative drugs except Zanamivir
http://en.wikipedia.org/wiki/Oseltamivir
Pros and Cons
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13 G
1.3 G 10 capsules of Tamiflu (75mg)
http://en.wikipedia.org/wiki/Star_anise
From current industrial process
Synthesis Issue: 1) Streamlining synthesis2) Greener synthesis3) Large-Scale manufacturing - overall steps, cost, starting material availability, protecting group, halogenated solvents, hazardous and toxic reagents, chromatography, etc..
(Star Anise) Shikimic acid
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Gilead Science’s First Total Synthesis: the use of (‒)-Shikimic acid
Kim, C. U.; Lew, W.; Williams, M. A.; Liu, H.; Zhang, L.; Swaminathan, S.; Bischofberger, N.; Chen, M. S.; Mendel, D. B.; Tai, C. Y.; Laver, W. G.; Stevens, R. C. J. Am. Chem. Soc. 1997, 119, 681.
HO
HO
OH
CO2H PPh3, DEAD HO CO2MeEsterification
O
1) MOMCl, 97%2) NaN3,86% MOMO CO2Me
HO
N3
1) MsCl, TEA, 99%
2) PPh3, 0 oC, 3 h
then TEA, H2O, 78%MOMO CO2Me
HN
1) NaN3, DMF, 77%2) HCl, MeOH, 99%
77%
HO CO2Me
H2N
N3
1) TrCl, TEA
2) MsCl, 0 oC, 22h
86% for 2 steps
CO2Me
TsN
N3
1) BF3OEt2 , 3-pentanol, 70 oC
2) Ac2O, DMAP, Pyridine
69% for 2 steps
CO2Me
AcHN
N3
O
1) PPh3
THF/H2O, 90%2) KOH, r.t.then Dowex
CO2H
AcHN
NH2
O
14 steps, 15% overall
Shikimic acid
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F. Hoffman-La Loche’s current process
Abrecht, S.; Harrington, P.; Iding, H.; Karpf, M.; Trussardi, R.; Wirz, B.; Zutter, U. Chimia 2004, 58, 621.
Federspiel M., Fischer R., Hennig M., Mair H.-J., Oberhauser T., Rimmler G., Albiez T., Bruhin J., Estermann H. et al. Org. Process Res. Dev. 1999, 3, 266–274.
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F. Hoffman-La Loche Ltd.: new method8 Steps, 20% overall
Karpf, M.; Trussardi, R. Angew. Chem., Int. Ed. 2009, 48, 5760.
1) Two azide substitution 2) operational simplicity, inexpensive route, no protecting group
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Corey’s Approach: EnantioselectiveDiels-Aler Reaction
Yeung, Y.-Y.; Hong, S.; Corey, E. J. J. Am. Chem. Soc. 2006, 128, 6310
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Shibasaki’s First Approach: Y-catalyzed asymmetric opening of aziridine
Y. Fukuta, T. Mita, N. Fukuda, M. Kanai, M.Shibasaki, J. Am. Chem. Soc. 2006, 128, 6312.
HN
N3
O NO2
NO2
96 %, 91 % ee
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1) Catalytic asymmetric introductionof 1,2-diamine functionality2) Relatively long overall steps, low overallyield3) Protection/ Deprotection4) Mitsunobu reaction5) Toxicity of SeO2
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Shibasaki’s second Approach: Diels-Alder reaction
Yamatsugu, K.; Yin, L.; Kamijo, S.; Kimura, Y.; Kanai, M.; Shibasaki, M. Angew. Chem., Int. Ed. 2009, 48, 1070.
Yamatsugu, K.; Kanai, M.; Shibasaki, M. Tetrahedron 2009, 65, 6017.
1) Scalable2) Curtius rearrangement3) Several chromatography includingPrep-TLC4) Overall 13%, 11 steps
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Satoh, N.; Akiba, T.; Yokoshima, S.; Fukuyama, T. Angew. Chem., Int. Ed. 2007, 46, 5734
Fukuyama’s approach: Enantioselective Diels-Alder reaction
5.6%, 14 steps
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Wong’s synthesis
Shie, J.-J.; Fang, J.-M.; Wong, C.-H. Angew. Chem., Int. Ed. 2008, 47, 5788
Chemoenzymatric oxidationOf bromobenzene
Use of strong base
Mitsunobu
11steps, 21-26%
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Hayashi’s approach: two “one-pot” sequence
Ishikawa, H.; Suzuki, T.; Orita, H.; Uchimaru, T.; Hayashi, Y. Chem. Eur. J. 2010, 16, 12616.
One pot from 134
Use of equimolar 136 and 137
The formation of single diastereomer141
Ishikawa, H.; Suzuki, T.; Hayashi, Y. Angew. Chem., Int. Ed. 2009, 48, 1304
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Hayashi’s approach: two “one-pot” sequence (cont’d)
1) 10 overall steps, 60% overall yield, deomstrated on gram-scale2) Protecting group free, base free, no chromatography, no purification of intermediates
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Hayashi’s approach: Preparation of Starting materials
Patented!!
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Trost, B. M.; Zhang, T. Angew. Chem., Int. Ed. 2008, 47, 3759
Trost’s Synthesis: AAA chemistry
Two Trasition metal catalyzed transformation1) Pd-catalyzed AAA2) Rh-catalyzed aziridination
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Trost’s Synthesis: AAA of lactone
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Hudlicky’s First Approach using ethyl benzoate
Sullivan, B.; Carrera, I.; Drouin, M.; Hudlicky, T. Angew. Chem.,Int. Ed. 2009, 48, 4229.
1) Chemoenzymatic Approach from readilyavailable ethyl benzoate ($30/1Kg) 2) Diels-Alder reaction to introduce aminogroup at C43) The use of azide, low yielding enzymaticoxidation, overall 10% to the compound 14
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Hudlicky’s Second Approach using ethyl benzoate
1) Azide Free synthesis2) Safty concern: NH2OH-HCl3) Scalability of Mitsunobu?4) Several chromatography and mg scaleSynthesis in the experimental procedure.
Werner, L.; Machara, A.; Hudlicky, T. Adv. Synth. Catal. 2010,352, 195−200.
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Ma’s approach: Organocatalysis
Zhu, S.; Yu, S.; Wang, Y.; Ma, D. Angew. Chem., Int. Ed. 2010, 49, 4656.
5 steps,46% !!
Preinstallation of diamine moiety- Azide free synthesis
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Ma’s approach: Preparation of 2-aminonitroolefin
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Raghavan’s asymmetric Diels-Alder approach
Raghavan, S.; Babu, V. S. Tetrahedron 2011, 67, 2044.
Starting from the chiral acid
Mitsunobu to installC3-amino group
Carbamate-directedEpoxidation
16 Steps, 4.3%
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Asymmetric Diels-Alder reaction
Poll, T.; Sebezak, A.; Hartmann, H.; Helmchen, G. Tetrahedron Lett. 1985, 26, 3095.
100 G/ $ 274recyclable
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1) Use of ChiralSulfinamide to installdiastereoselectiveamine functionality
2) 11 steps21% overall
D-tartrate: $213/ 100G
Lu’s approach: D-Tartrate
Weng, J.; Li, Y.-B.;Wang, R.-B.; Li, F.-Q.; Liu, C.; Chan, A. S. C.; Lu, G. J. Org. Chem.2010, 75, 3125.
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Ko’s approach: D-mannitol
Ko, J. S.; Keum, J. E.; Ko, S. Y. J. Org. Chem.2010, 75, 7006.
1) Sharpless dihydroxylationAzide chemistry in hight temp.Chromatographic separationProtecting group
2) 16 steps/ 7% overall
D-mannitol: $163/ 3 KG - attractive starting material
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Chen and Chai’s Formal synthesis: D-Ribose
Osato, H.; Jones, I. L.; Chen, A.; Chai, C. L. L. Org. Lett. 2010, 12, 60.
1) Protecting group free,but halogenated solventchromatography
2) 12 steps/ 9% overall
D-Ribose: $250/ 0.5 KG
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Chuanopparat, N.; Kongkathip, N.; Kongkathip, B. Tetrahedron 2012, 68, 6803-6809
Kongkathip’s approach: D-mannose
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Kongkathip’s approach: D-mannose (cont’d)
11 steps, 2.9% overall
D-mannose: $312/ 0.5 KG
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SUMMARY
HO
HO
OH
CO2H
Shikimic acid
Hoffman-La Loche
HN
N3
O NO2
NO2
Shibasaki Wong
Hayashi
Ma
OH
OH
Br
Hudlicky Lu
Asymmetric Organocatalysis
OH
OH
EtO2C
EtO2C
D-tartrate
HOOH
OH
OH
OH
OH
D-mannitol
Ko
O OH
HO OH
HO
D-ribose
Chen and Chai
O
HO
OH
OH
OHHO
D-mannose
Kongkathip
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Corey
ShibasakiFukuyama
Asymmetric Diels-Alder Strategy
CO2H
O
O
O
O
Raghavan
SUMMARY (cont’d)
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SUMMARY (cont’d)
Need to keep developing total synthesis?
Yes. The mutation of influenza virus (e.g. H5N1) is probable to make a global pandemic in the future. New drug development for the alternative of Oseltamivir also required for drug-resistant viruses.
New and economic process to manufacture this drug may help decrease the price, which ultimately helps people in developing countries.
The patent expires in 2016, thus efficient and inexpensive production of this drug will determine the market price.
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HO
HO
OH
CO2H
PPh3, DEAD HO CO2MeEsterification
O
1) MOMCl, 97%2) NaN3,86%
MOMO CO2Me
HO
N377%
Shikimic acidA
1)
SPh
CO2EtO
NO2
ClO2C
1) TMSN3, pyridine, toluene
SPh
CO2EtO
NO2O
N3
2) Ac2O, HOAc
SPh
CO2EtO
NO2
NC
O
O
OH
SPh
CO2EtO
NO2NHO
OO
SPh
CO2EtO
NO2NH
O
-CO2
2)
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3) Proposed catalytic cycle