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![Page 1: Combinations of Enzymatic Procedures with Multicomponent Condensations Ryszard Ostaszewski a,b a Faculty of Chemistry, Warsaw University of Technology,](https://reader031.fdocuments.us/reader031/viewer/2022013012/5697bf991a28abf838c916cc/html5/thumbnails/1.jpg)
Combinations of Enzymatic Procedures with
Multicomponent Condensations
Ryszard OstaszewskiRyszard Ostaszewskiaa,b,b
aa Faculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, 00-664 WarszawaFaculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, 00-664 Warszawa
bb Institute of Organic Chemistry, PAS, Kasprzaka 44/52, 01-224 Institute of Organic Chemistry, PAS, Kasprzaka 44/52, 01-224 Warszawa, PolandWarszawa, Poland
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General concept. CClassical processes:lassical processes:
Substrate(racemic)
Resolution of enantiomers
Substrate (optically
active)
Reaction 1
Product Reaction 2
Final product
Combination of Enzymatic Procedures with multicomponent condensation.
Substrate(meso)
Enzymatic Reaction (1)
Product Multicomponent condensation. (2)
Final product
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General requirements for whole processes:General requirements for whole processes: - possibility to perform both reaction as a two - step one - pot procedure,- possibility to perform both reaction as a two - step one - pot procedure, - economy and simplicity,- economy and simplicity, - easy control of the stereochemical course of reactions. - easy control of the stereochemical course of reactions.
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Multicomponent Condensations Ugi reactionUgi reaction
Bu NH2
O
H CNN
O
N
O
HO
OH
+ + +
Passerini reaction
O
H CNN
O
O
O
HO
OH+ +
Petasis reaction
R1
O
OHO
N
OH
O
RR
R1BOH
OH
RN
R
H+ +
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EtO OH
O O
Cl
Cl
Holmann, M. J.; Vail, R.; Morgan, B., Sebesan, V.; Levy, C.; Dodds D. R.; Zaks, A.; Adv. Synth. Catal. 2001, 343, 744
ParoxetinParoxetin Yu, M. S.; Lantos, I.; Zhi-Qiang Peng, Yu J.; Cacchio T. Yu, M. S.; Lantos, I.; Zhi-Qiang Peng, Yu J.; Cacchio T. Tetrahedron Lett.Tetrahedron Lett. 20002000, 41, , 41,
5647.5647.
EtO OH
O O
F
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Synthetic strategy.
OO O
R
O OH
O O
R
R'
O X
O O
R
R'
R
O
NR
H+ ROH
Enzyme UGI (X= NR)
Passerini (X= O)
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The synthesis of 3-phenylglutaric anhydrides
R
O
O O
O
OO
Et
Et
HO OH
OO
R
OO O
R
HO OR'
O O
R
O
H
RO O
OEt
1a R=H1b R=Cl1c R=OMe
2 3
R'OH, Py
reflux, 2h
4
+piperidine
KOH
85-90oC
AcCl
5 R' =, Me, Et, Bu, Bn
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Desymmetrization of 3-phenylglutaric anhydrides
OO O
R
O OH
O O
Et
R
+ EtOH
R = H R = Cl R = Me
Solvent Time(h)
Er Time (h/days)
Er Time (days)
Er
1 diethyl ether 114 7,2 -/17 2,5
2 diisopropyl ether 43 8,2 120/- 5,2 22 5,4
3 di-n-propyl ether 177 8,0 -/17 5,3
4 di-n-butyl ether 73 6,9 72/- 5,1
5 tertbutyl methyl ether 43 7,3 120/- 3,6 14 5,6
6 Cyclohexane 20 4,3 72/- 1,1
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The influence of enzyme type on desymmetrization reaction.
R = H R = Cl R MeOLipase Time
(h/days)Er Time
(h/days)Er Time
(h/days)Er
Novozyme 435 61/- 8,5 120/- 5,2 -/22 5,4Chirazym A 19/- 10,8 -/4 5,9 -/12 6,4
Chirazym B -/9 0,80 -/4 0,7
Chirazym C -/18 5,2
Amano PS -/16 0,13
Amano PS imm. 19/- 0,13 -/4 1,4 -/7 267
SP 430 67/- 5,4 -/5 2,6
Candida cylindracea imm. -/46 1,62
Pseud. capacia imm. -/46 0,29
hog pancreas imm. -/18 0,88
Mucor miehei imm. -/46 0,35
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The results of combination of enzymatic desymmetrization with Ugi Four-Component Condensation.
OO O
R
O OH
O O
R
R'O N
O O
R
R'
R
R
O
NR
H+ ROH
EnzymeRNH2
RCHO
RNC
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O
O
N
OO
N
O
EtO
H
O
O
N
OO
N
O
EtO
H
O
O
N
OO
N
O
EtO
H
Entry Product Solvent Yield (%)
1
i-Pr2O
0
2 i-Pr2O/MeOH, 2:1,
v/v
6
3
i-Pr2O/MeOH
2:1, v/v
4
4
i-Pr2O/MeOH
2:1, v/v
6a
5
i-Pr2O/MeOH
2:1, v/v
13a
O
O
N
OO
N
O
EtO
H
O
O
N
OO
N
O
EtO
H
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Entry Product
Solvent Yield (%)
1
i-Pr2O/MeOH
2:1, v/v
82
2
i-Pr2O/MeOH
2:1, v/v
81a
3
i-Pr2O/MeOH
2:1, v/v
70 a
4
i-Pr2O/MeOH
2:1, v/v
72 a
5
i-Pr2O/EtOH
2:1, v/v
80 a
N
OO
N
O
EtO
H
N
OO
N
O
EtO
H
N
OO
N
O
EtO
Cl
H
N
OO
N
O
EtO
OMe
H
N
O
NO
O O H
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Passerini Reaction of 3-phenylglutaric monoesters
OO O
O OH
O O
RO O
O O
R
R1
O
NR
1
HROH
Lipase
1 2 3
R1CHO, R2NC
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Entry Product Solvent Yield (%)
1 i-Pr2O/EtOH
2:151
2
i-Pr2O/EtOH
2:1
46a
3 i-Pr2O/EtOH
2:135
4i-Pr2O/EtOH
2:1
56 a
5
i-Pr2O/EtOH
2:135
6 i-Pr2O/EtOH
2:1
50a
7
i-Pr2O/EtOH
2:118%
O O
O O
NH
O
O O
O O
NH
O
O O
O O
NH
O
O O
O O
NH
O
O O
O O
NH
O
C7H15
O O
O O
NH
O
C7H15
O O
O O
NH
O
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enzymatic reactions can be used with multicomponent Ugi and enzymatic reactions can be used with multicomponent Ugi and Passerini condensations as a two-step one-pot processesPasserini condensations as a two-step one-pot processes..
Summary
Acknowledgments
This work was supported by the State Commitee for Scientific Research (Grant 3 TO9A 081-19).
Katarzyna Jeziorska, Anna Fryszkowska, Marta Głażewska Katarzyna Jeziorska, Anna Fryszkowska, Marta Głażewska