Enamine diazoalkanes 2014

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CF3CHN2, C2F5CHN2:underestimated reagents

for organic synthesis

(Enamine Ltd, Kyiv, Ukraine)

Dr. Pavel Mykhailiuk

Kyiv

www.enamine.net

World's largestproducer of building blocks

Founded in 1991

www.enamine.net

100.000 building blocksin stock

It will take 300 years to test the whole collection,

when using 1 building block a day.

Founded in 1991

www.enamine.net 5

“~20% of drugs contain Fluorine”

S. Purser at al. Chem. Soc. Rev. 2008, 320 (rev.)

VinflunineFabre, 1998

CitafloxacineDaiichi, 2008

CarmegliptinRoche, 2010

VinflunineFabre, 1998

www.enamine.net 6

“Industrial production of drugs needspractical reactions”

S. D. Roughley et al. J. Med. Chem. 2011, 3451 (rev.)

www.enamine.net 7H. Gilman, R. G. Jones JACS, 1943, 1458.

For 60 years CF3CHN2 was rarely used in chemistry.

www.enamine.net 8

19F-label for Proline

2008

P. Mykhailiuk et al. ACIE 2008, 5765.

19F

www.enamine.net 9P. Mykhailiuk et al. ACIE 2008, 5765.

www.enamine.net 10

Ar

www.enamine.net 11

Advanced amines fordrug discovery

O. Artamonov et al. EurJOC 2014, 3592.

www.enamine.net 12O. Artamonov et al. EurJOC 2014, 3592.

X-Ray

CuClCF3CHN2

25%NBoc

OH

NBoc

NBoc

F3C H

HNH

F3C H

H

TFA

1. TosCl2. KOtBu

55%

N

F3C

Boc

Pd/C, H2 quant.

HCl

MeOHNH

F3C

quant.

92%

CH2Cl2 CH2Cl2

MeOH

www.enamine.net 13O. Artamonov et al. EurJOC 2014, 3592.

www.enamine.net 14

CF3CHN2 (gas)

CuClEDG

F3C

EDG

EDG: electron-donatinggroup

O. Artamonov et al. EurJOC 2014, 3592.P. Mykhailiuk et al. Synthesis 2008, 1741.P. Mykhailiuk et al. ACIE 2008, 5765.

www.enamine.net 15O. Artamonov et al. EurJOC 2014, 3592.P. Mykhailiuk et al. Synthesis 2008, 1741.P. Mykhailiuk et al. ACIE 2008, 5765.

www.enamine.net 16

Easy to do

No purification

Scalable (1g-5g-10g)

One-pot, RT, no inert atmosphere, no catalysts,common solvents,no gaseous reagents,no side products,100% yield

www.enamine.net 17E. Slobodyanyuk et al. EurJOC 2014, 2487.

www.enamine.net 18E. Slobodyanyuk et al. EurJOC 2014, 2487.

www.enamine.net 19

For unclear reasonsC2F5CHN2 was unknown

www.enamine.net 20P. Mykhailiuk Chem. Eur. J. 2014, 4942.

www.enamine.net 21P. Mykhailiuk Beilstein JOC 2014, in press.

www.enamine.net 22

www.enamine.net 23

“Production of drugs and argochemicalsneeds fluorinated molecules

and practical reactions”

S. D. Roughley et al. J. Med. Chem. 2011, 3451 (rev.) S. Purser at al. Chem. Soc. Rev. 2008, 320 (rev.)

www.enamine.net 24

www.enamine.net 25H. Gilman, R. G. Jones JACS, 1943, 1458.

For 60 years CF3CHN2 was rarely used in chemistry.

However, during the past 5 years, in-situ generated CF3CHN2was used in more than 70 papers:

Prof. G. Simonneaux, Prof. E. Carreira, Prof. J.-A. Ma,Prof. D. Cahard,Prof. W. Xiao,Prof. M. Duncton, Prof. G. Molander,Prof. J. Wang.

www.enamine.net

AcknowledgementEvgeniy Slobodyanyuk

Olexyi Artamonov

Prof. Anne UlrichProf. Igor KomarovProf. Olha ZaporozhetsProf. Andrey Tolmachev500 chemists

O. Ishenko, V. Stepanenko

(synthesis of C2F5CH2NH2)

Unique alkynes and alkenes were synthesized by our chemists at Enamine.

www.enamine.net

CF3CHN2, C2F5CHN2:underestimated reagents

for organic synthesis

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