3-Pyrrolidinecarboxylic acid for direct catalytic asymmetric anti-Mannich-type reactions of unmodified ketones

Article abstract of DOI:10.1021/ja062950b

We report the development of direct catalytic, enantioselective, anti-selective Mannich-type reactions between unmodified ketones and α-imino esters under mild conditions. The reactions were performed using 5-10 mol % of (R)-3-pyrrolidinecarboxylic or (R)-β-proline as catalyst in an environmentally benign solvent, 2-PrOH, at room temperature. The anti-Mannich products were obtained in good yields with high diastereo- and enantioselectivities (up to anti/syn >99:1, 99% ee). While (3R,5R)-5-methyl-3-pyrrolidinecarboxylic acid is an excellent catalyst for the anti-Mannich-type reactions of aldehydes, it did not efficiently catalyze the corresponding Mannich-type reactions of ketones; (R)-3-pyrrolidinecarboxylic acid did efficiently catalyze the Mannich-type reactions of ketones. (S)-Proline or (S)-2-pyrrolidinecarboxylic acid has been reported to catalyze the Mannich-type reactions of ketones to afford the syn-products. Thus, the position of the carboxylic acid group on the pyrrolidine ring directs the stereoselection of the catalyzed reaction, providing either syn- or anti-Mannich products. Copyright

Full text of DOI:10.1021/ja062950b

Published on Web 07/11/2006
3-Pyrrolidinecarboxylic Acid for Direct Catalytic Asymmetric
anti-Mannich-Type Reactions of Unmodified Ketones
Haile Zhang, Maria Mifsud, Fujie Tanaka,* and Carlos F. Barbas, III*
The Skaggs Institute for Chemical Biology and the Departments of Chemistry and Molecular Biology, The Scripps
Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037
Received April 27, 2006; E-mail: ftanaka@scripps.edu; carlos@scripps.edu
Scheme 1
Asymmetric Mannich and Mannich-type reactions are important
carbon-carbon bond-forming reactions that provide access to
enantiomerically enriched â-amino carbonyl derivatives.1-8 The
most desired versions are direct catalytic reactions that afford the
syn- or anti-products with high diastereo- and enantioselectivities.1
Methods that use unmodified aldehydes and ketones are more atom-
economical than those that require preactivation of carbonyl
compounds, such as preformation of silyl enol ethers. For Mannich
or Mannich-type reactions involving unmodified aldehydes, both
syn-2 and anti-selective3 methods that afford products with high
enantioselectivity have been reported; for example, pyrrolidine
derivatives and related amines have been used as catalysts.2,3 For
the reactions involving unmodified ketones, methods affording syn-
Mannich products have been reported,2b,4 but routes to the anti-
products with high levels of diastereo- and enantioselectivities are
limited to the reactions of R-hydroxyketones using Zn catalysts1b,5
and the reactions of â-ketoesters using cinchona alkaloids.6 Other
examples of highly enantioselective anti-selective Mannich reactions
of ketones use silyl enol ethers rather than unmodified ketones.7
Here we report Mannich-type reactions between unmodified ketones
and N-p-methoxyphenyl (PMP)-protected R-imino esters that afford
anti-products with high diastereo- and enantioselectivities, using
â-proline or 3-pyrrolidinecarboxylic acid (1) as catalyst.
We recently designed an anti-Mannich catalyst, (3R,5R)-5-
methyl-3-pyrrolidinecarboxylic acid (2), and demonstrated the
highly diastereo- and enantioselective anti-Mannich-type reactions
of aldehydes using this catalyst (Scheme 1a).3a We suggested that
key for the formation of anti-Mannich products is the use of
Table 1. Evaluation of Catalysts for the anti-Selective
enamine conformation A over B in the C-C bond-forming
Mannich-Type Reaction of 3-Pentanonea
transition state.3a Catalyst 2, however, was ineffective in the
Mannich-type reactions of ketones. The 2-catalyzed Mannich-type
reaction between 3-pentanone and N-PMP-R-imino ethyl glyoxylate
was very slow (Table 1, entry 1). Upon consideration of the
transition states of the ketone reaction, we reasoned that the low
efficiency of catalyst 2 in the ketone reaction originated from
relatively slow formation of the enamine intermediates due to steric
interaction with the methyl group of the catalyst (Scheme 1b). Note
that proline does catalyze the syn-Mannich-type reactions of both
aldehydes2a and ketones4a-c (Scheme 1c).
entry
catalyst
time
yieldb (%)
drc anti/syn
major anti-4
eed (%)
1
2
3
2
3 d
29 h
3 d
<10
75
83
(R)-1
(S)-3
94:6
94:6
(2S,3R)
(2R,3S)
97
85
In the case of the Mannich-type reactions of isovaleraldehyde,
although both the 3-carboxylic acid and 5-methyl groups of catalyst
2 were critical for excellent anti-selectivity and enantioselectivity,
the 3-carboxylic acid group alone had a significant role in the
stereoselection.3a We reasoned that unmethylated catalyst (R)-3-
pyrrolidinecarboxylic acid ((R)-1) should afford anti-Mannich
products in the ketone reactions; although enamine conformations
C and D may have similar free energies, only C should advance to
the C-C bond formation via transition state E (Scheme 1d). When
proton transfer occurs from the acid at the 3-position of the catalyst
to the imine nitrogen, the nucleophilic carbon of enamine C should
a To a solution of N-PMP-protected R-imino ester (0.5 mmol, 1 equiv)
and 3-pentanone (2.0 mL, 19 mmol, 38 equiv) in anhydrous DMSO (3.0
mL), catalyst (0.1 mmol, 0.2 equiv, 20 mol % to the imine) was added,
and the mixture was stirred at room temperature (25 °C). b Isolated yield
(containing anti- and syn-diastereomers). c Determined by HPLC before
purification. d Determined by chiral-phase HPLC for anti-4.
be properly positioned to react with the imine, whereas the
nucleophilic carbon of enamine D should be too far from the imine
carbon to form a bond. Since 1 does not have an R-substituent on
the pyrrolidine, neither enamine C nor D has a disfavored steric
9
9630
J. AM. CHEM. SOC. 2006, 128, 9630-9631
10.1021/ja062950b CCC: $33.50 © 2006 American Chemical Society

C O M M U N I C A T I O N S
Table 2. (R)-1-Catalyzed anti-Mannich-Type Reactions of
Table 3. (R)-1-Catalyzed anti-Mannich-Type Reactions of Cyclic
Ketonesa
Ketonesa
time
(h)
yieldb
(%)
drc
anti/syn
eed
(%)
R1
R2
R3
product
catalyst
(equiv)
yieldb
(%)
drc
anti/syn
eed
(%)
entry
entry
X
R
product
1
Et
Me
Me
Me
Et
Et
20
48
t-Bu 20
4
4
5
6
7
91
77
93
76
85f
97:3
97:3
97
98
95
82
90
1e CH2
2
3
Et
i-Pr
t-Bu
0.1
0.05
0.05
11
12
13
96 >99:1 96
94 >99:1 94
92 >99:1 95
2e Et
CH2
CH2
3
4
5
Et
n-Pr Et
Me Me
>99:1
>99:1
∼10:1
Et
Et
96
5
(99)f
4
5
6
7
8
9
CH2
S
S
O
CH2CHdCH2 0.05
14
15
15
16
17
17
95 >99:1 95
78 >99:1 99
71 >99:1 97
82 >95:5 86
87 >99:1 97
80 >99:1 96
(>99:1)g (>99)g
Et
Et
Et
0.1
0.05
0.1
0.1
0.05
6h Me Me
Et
Et
5
ent-7
81f
∼10:1
(>99:1)g
∼10:1
88
(99)g
92
91
84
7
8
9
Me Et
Me CH2CHdCH2 Et
Me (CH2)3Cl Et
10
14
14 10
8
9
81f
85
68
C(OCH2)2 Et
C(OCH2)2 Et
>95:5
>95:5
a Typical conditions: imine (0.5 mmol, 1 equiv), ketone (1.0 mmol, 2
a Typical conditions: to a solution of imine (0.5 mmol, 1 equiv) and
equiv), (R)-1 (0.05 mmol, 0.1 equiv or 0.025 mmol, 0.05 equiv), and 2-PrOH
(1.0 mL), 25 °C. b Isolated yield. c Determined by NMR of isolated products.
d Determined by chiral-phase HPLC of the anti-product. e Ketone (5.0 mmol,
10 equiv) was used. f Data after crystallization.
ketone (5.0 mmol, 10 equiv) in 2-PrOH (1.0 mL), (R)-1 (0.05 mmol, 0.1
equiv) was added, and the mixture was stirred at 25 °C. b Isolated yield
(containing anti- and syn-diastereomers). c Determined by NMR of isolated
products. d Determined by chiral-phase HPLC for the anti-product. e Ketone
(4 equiv) and (R)-1 (0.05 equiv) at 4 °C. f Containing regioisomer (∼5-
10%). g Data after crystallization are shown in parentheses. The dr was
determined by HPLC. h Catalyst (S)-1 was used.
Acknowledgment. This research was supported in part by The
Skaggs Institute for Chemical Biology. We thank Dr. Raj K. Chadha
for X-ray structural analysis.
interaction like the one shown in Scheme 1b and enamine formation
of ketones with 1 should be faster than that with 2.
Supporting Information Available: Experimental procedures,
characterization data, spectral data, and X-ray crystal structures of 7
and 13. This material is available free of charge via the Internet at
http://pubs.acs.org.
In fact, the (R)-1-catalyzed reaction was significantly faster than
the 2-catalyzed reaction and afforded the anti-Mannich product
(2S,3R)-4 in good yield with high diastereo- and enantioselectivities
(Table 1, entry 2), supporting our design considerations. When the
position of the carboxylic acid group on the pyrrolidine ring was
changed from the 2- to the 3-position (that is, from proline to cata-
lyst 1), the stereochemistry of the product of the catalyzed reaction
was altered from syn to anti. Catalyst (S)-3, which possesses a sul-
fonamide group, also catalyzed the reaction and afforded the anti-
product, but the reaction catalyzed by 1 was faster and afforded
higher enantioselectivity than the 3-catalyzed reaction. These results
indicate that the acid functionality at the 3-position on the pyrroli-
dine ring plays an important role in properly positioning the imine,
as shown in Scheme 1d, for a faster reaction rate and for affording
the anti-products with high diastereo- and enantioselectivities.
Evaluation of the (R)-1-catalyzed reaction to afford (2S,3R)-anti-4
in various solvents at room temperature showed that the reaction
in 2-PrOH provided the highest reaction rate, yield, anti-selectivity,
and enantioselectivity of the solvents tested (Table 2, entry 1 and
Supporting Information).
Amino acid (R)-1 catalyzed Mannich-type reactions between a
variety of ketones and R-imino esters and afforded the anti-products
in good yields with high diastereo- and enantioselectivities in most
cases (Tables 2 and 3). For the reactions of unsymmetrical methyl
alkyl ketones, the reaction occurred predominantly at the more
substituted R-position of the ketones (Table 2, entries 5-9). The
regio-, diastereo-, and enantiomeric purities of the anti-products
were readily improved by crystallization (Table 2, entries 5 and 6
and Table 3, entry 3). For the reactions of six-membered cyclic
ketones, use of only 5 mol % of catalyst 1 and 2 equiv of ketone
to the imine afforded the desired anti-products in good yields within
approximately 12 h.
References
(1) (a) Kobayashi, S.; Ishitani, H.; Ueno, M. J. Am. Chem. Soc. 1998, 120,
431. (b) Matsunaga, S.; Yoshida, T.; Morimoto, H.; Kumagai, N.;
Shibasaki, M. J. Am. Chem. Soc. 2004, 126, 8777.
(2) (a) Notz, W.; Tanaka, F.; Watanabe S.; Chowdari, N. S.; Turner, J. M.;
Thayumanuvan, R.; Barbas, C. F., III. J. Org. Chem. 2003, 68, 9624 and
references therein. (b) Cobb, A. J. A.; Shaw, D. M.; Ley, S. V. Synlett
2004, 558.
(3) (a) Mitsumori, S.; Zhang, H.; Cheong, P. H.-Y.; Houk, K. N.; Tanaka,
F.; Barbas, C. F., III. J. Am. Chem. Soc. 2006, 128, 1040. (b) Kano, T.;
Yamaguchi, Y.; Tokuda, O.; Maruoka, K. J. Am. Chem. Soc. 2005, 127,
16408. (c) Franzen, J.; Marigo, M.; Fielenbach, D.; Wabnitz, T. C.;
Kjaersgaard, A.; Jorgensen, K. A. J. Am. Chem. Soc. 2005, 127, 18296.
(d) Cordova, A.; Barbas, C. F., III. Tetrahedron Lett. 2002, 43, 7749.
(4) (a) Notz, W.; Watanabe, S.; Chowdari, N. S.; Zhong, G.; Betancort, J.
M.; Tanaka, F.; Barbas, C. F., III. AdV. Synth. Catal. 2004, 346, 1131
and references therein. (b) Westermann, B.; Neuhaus, C. Angew. Chem.,
Int. Ed. 2005, 44, 4077. (c) Enders, D.; Grondal, C.; Vrettou, M.; Raabe,
G. Angew. Chem., Int. Ed. 2005, 44, 4079. (d) Wang, W.; Wang, J.; Li,
H. Tetrahedron Lett. 2004, 45, 7243. (e) Trost, B.; Terrell, L. R. J. Am.
Chem. Soc. 2003, 125, 338. (f) Sugita, M.; Yamaguchi, A.; Yamagawa,
N.; Handa, S.; Matsunaga, S.; Shibasaki, M. Org. Lett. 2005, 7, 5339. (g)
List, B. J. Am. Chem. Soc. 2000, 122, 9336.
(5) Trost, B. M.; Jaratjaroonphong, J.; Reutrakul, V. J. Am. Chem. Soc. 2006,
128, 2778.
(6) Lou, S.; Taoka, B. M.; Ting, A.; Schaus, S. J. Am. Chem. Soc. 2005,
127, 11256.
(7) (a) Ferraris, D.; Young, B.; Cox, C.; Drury, W. J., III; Dudding, T.; Lectka,
T. J. Org. Chem. 1998, 63, 6090. (b) Ferraris, D.; Young, B.; Cox, C.;
Dudding, T.; Drury, W. J., III; Ryzhkov, L.; Taggi, A. E.; Lectka, T. J.
Am. Chem. Soc. 2002, 124, 67. (c) Hamada, T.; Manabe, K.; Kobayashi,
S. J. Am. Chem. Soc. 2004, 126, 7768.
(8) (a) Song, J.; Wang, Y.; Deng, L. J. Am. Chem. Soc. 2006, 128, 6048. (b)
Poulsen, T. B.; Alemparte, C.; Saaby, S.; Bella, M.; Jorgensen, K. A.
Angew. Chem., Int. Ed. 2005, 44, 2896. (c) Hamashima, Y.; Sasamoto,
N.; Hotta, D.; Somei, H.; Umebayashi, N.; Sodeoka, M. Angew. Chem.,
Int. Ed. 2005, 44, 1525. (d) Hayashi, Y. Urushima, T.; Shoji, M.;
Uchimaru, T.; Shiina, I. AdV. Synth. Catal. 2005, 347, 1595. (e) Uraguchi,
D.; Terada, M. J. Am. Chem. Soc. 2004, 126, 5356. (f) Akiyama, T.; Itoh,
J.; Yokota, K.; Fuchibe, K. Angew. Chem., Int. Ed. 2004, 43, 1566. (g)
Josephsohn, N. S.; Snapper, M. L.; Hoveyda, A. H. J. Am. Chem. Soc.
2004, 126, 3734. (h) Wenzel, A.; Jacobsen, E. N. J. Am. Chem. Soc. 2002,
124, 12964.
In summary, we have developed the (R)-1- and (S)-1-catalyzed
anti-selective Mannich-type reactions of unmodified ketones that
afford high diastereo- and enantioselectivities. We have demon-
strated that the position of the acid group on the pyrrolidine ring
directs the stereoselection of the catalyzed reaction, providing either
syn- or anti-Mannich products.
JA062950B
9
J. AM. CHEM. SOC. VOL. 128, NO. 30, 2006 9631