Solution and Solid Phase Synthesis of Unusual a-Amino Acids From

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5-430 (2S)-2-Amin013-hydn,xgbutanedioic acid, Asp(p-OWH, 5.5- Same procedure as in section 5.4.14 to give 0.029 g (62%) of 53. "XCO*" H2 C02H 2S,3S-5.5: [a120~ = 4.4 (c = 1.5, 1N HCl), (lit." = +1.3 (c = 3.12, 1N HCI); 'H NMR (D20.300 MHz) 6 4.89 (d. 1 H, J = 3.6Hz, p-CH) 3.82 (d, 1 H, J = 3.6Hz, a-CH); 13c NMR (&O, 75 MHz) 6 178.2 -1, 173.7 cd), 69.3 (p-CH), 61.5 (a-CH); ESI- MS 149.91. 5-4-21 1 -[(2S)-2-[(Be11~yloxy)~bo~y1]smin011-(rne~yl- 2,6,7-trioxabicyclo[2.2.2 Joct-l-yl)ethyl]-l,2-~azadien-2-ium, Cbz-L-Asp(p- N3)(OMe)OBO ester, 5-53, Cbz-Asp(0Me)OBO ester 5-38 (0.370 g, 1.01 mmol) was dissolved in dry THF (3 rnL) then added by cannula to a Bask containing LiHMDS ( 3.03 rnL, 3.03 mmol) in dry TH. (5 mL) at -78°C under Ar. After 1 h. trisyl azide 4.105 (0.624 g, 2.02 mmol) dissolved in dry THF (3 mL) was slowly added by syringe. Mer 18 h at -78"C, the mixture was allowed to warm to room temperature then poured into Et20 (50 mL) and extracted with 3% NHKl (2 x 20 mL), 10% NaHCO3 (?O mL), brine (20 mL) and dried over MgS04 and the solvent removed under reduced pressure to give a bright yelIow oil which was purified by flash chromatography to give 5.53 in 28% yield (0.1 14 g).
TU3 ( 1 : 1, EtOAc:Hex), Rr = 0.40; 'H NMR (Acetone-&, 300 MHz) 6 7.37-7.22 (m, SH, ArH), 5.44 (d, lH, J = 10.2H2, NH), 5.07 (m, 2H, CbzCH20), 4.19 (dd, lH, J = 3.7, 10.2Hz, $-CH), 3.95-3.79 (s + m, 7H, OB0 ester CHD, &CH), 3.67 (S. 3H, C02CH3), 0.80 (s, 3H, OB0 ester CC&); 13c NMR (Acetone-d6, 75 MHz) 6 172.3 Ca), 156.6 (CONH), 136.4, (Cbz=C=), 128.2, 127.9, 127.6 (Ch-=), 108.1 (OB0 ester C-O), 72.3 (OB0 ester _&O), 66.8 (CbzCHzO), 59.9 @-CH), 52.1 (CO&H3), 52.2 (a-CH), 30.4 (OB0 ester CCH3), 14- 1 (OB0 ester Ca& FMR (cast fiom CH2C12) 3432, 2962, 2884,2122, 1729, 1515, 1048; ESI-MS (M + 406.91; Anal. caicd for C18H22N4@: C, 53.20; H, 5.46; N, 13.79. Found: C, 53.54; H, 5.85; N, 13.85. 5.4.22 Methyl-(~)-3-aminol21[(bellzyloxy)carbonyl]amin012-(4-methyl-2,6,7- trioxabicyclo[2.2.2]0~t-1-yl)pmpanoate, Cbz-L-Asp(B-NH2)(OMe)OB0 ester, 5.54. Cbz-L-Asp(P-N3)(OMe)OB0 ester 5.53 (0.1 14 g, 0.28 mrnol) was combined with PhsP (0.088 g, 0.33 mrnol) and dissolved in dry THF (5 rnL) then stirred at room temperature for 24 hours. Distilled water (20 pL) was then added and the mixture refluxed for 3 hours. The solvent was removed under reduced pressure to give a white solid that was purified by flash chromatography (9: 1, EtOAcMeOH 0.5% WOH) to give 5.54 in 67% yield (0.07 1 g).
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Solution and Solid Phase Synthesis
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The University of Waterloo requires
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Many people have made the experienc
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Table of Contents Abstract ........
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23 Summary ........................
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5.1.4.1 Enzymatic Methods .........
Page 13 and 14:
List of Tables Table 2.1 Table 2.2
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Figure 4.1 O Figure 5.1 Figure 5.2
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CYS d DAST DBAD DBU DCC de DEAD dec
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NMP Nu OB0 ester PEG Ph Phe PhFl Ph
Page 21 and 22:
1.1 General Introduction Chapter On
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acids will be presented including a
Page 25 and 26:
.J generation of the enolate and ad
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classical techniques (Scheme 1.7) a
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s~ccess.~ The same principle has be
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O Scheme 1.11 O R1,qH2 m OH RI= H,
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stereosele~tivities.~ Numerous exam
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Williams and coworlcers have examin
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template, reaction with alkyl halid
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The 3-bromo analog of Williams and
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formation of serine aldehydes; dire
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Scheme 1.24 R dimethoxy- R ProPane
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of thiol trityl led to racemic cyst
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nucleophiles such as acetate and im
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may be employed, while the oxidatio
Page 51 and 52:
Several methods for the removal of
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1.5 References Barrett, G.C. Chemis
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(a) Schmidt, U.; Meyer, R.; Leitenb
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R.M. Tetrahedron Le#. 2001,42, 769.
Page 59 and 60:
(a) Lubell, W.D.; Rapport, H. J. Am
Page 61 and 62:
Nakajima, K.; Takai, F.; Tanaka, T.
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2.1 Introduction Chapter Two Synthe
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2.1.1 Synthesis of SHydroxy-a-Amino
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typically generated in both poor yi
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2.1.3.3 Electrophilic%Nucfeophilic
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Scheme 2.8 2-(Arylthi0)-2-nitrooxir
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Scheme 2.10 Schollkopf et al. have
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2.1.3.5 Synthesis fiom #-Amino Acid
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HO Scheme 2.17 This laboratory prev
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Scheme 2.19 NaBr, acetone The best
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equires carefiil attention to preve
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order to investigate this as a poss
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etained its optical activity indica
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2.2.3.2 Ortho Ester Cleavage Concom
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2.2.4 Determination of Enantiomeric
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minof si face aîîack mior re face
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2.4.1 General Methods. Most reagent
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The crude product was fiitered thro
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250 MHz) 6 5.47 (br ci, lH, J = S.O
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evaporated to dryness. The residue
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minutes. The akohol solution was tr
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302.1604, found 302.1593; Anai. cal
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CCH3), 28.3 (a3)C), 20.1 (fLm3) 13.
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TLC (4: 1, CH2C12:EtOAc) Rf = 0.44;
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100-200 mesh, hydrogen form, 1x10 c
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(br d. IH. J= 10.6Hz, CHH-CH), 4.63
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mp 80-8 1 OC; [a~~*~a= -67.0 (0 1.5
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esin column (Bio-Rad AGa 10x4 10-20
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Jung, M.E.; Jung, Y.H. Tetruhedron
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(a) Adams, Z.M.; Jackson, R.F.W.; P
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(a) Roemmele, R.C.; Rapport, H. J.
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- - 68. Gawley, R.E.; Aubé, J. Pri
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pyridoxal phosphate dependent enzym
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Vinylglycines are also useful as sy
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In 1984, a modified Strecker synthe
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The main byproduct of elimination w
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, HO- OH Scheme 3.14 , 1) pb(OAc),
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L-vinylglycine has also been synthe
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Ser(a1d)-OB0 gave the desired olefi
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A tram relationship for H2IH3 in th
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33 Summary The Cbz OB0 ester protec
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67.1 (Ar_cH20), 63.2 @--a), 56.3 (a
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yielded a slightiy yellowish solid
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JAS Grigiarà ddition of trimethyls
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6 158.9 (CONH), 107.4 (OB0 ester C-
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Rutjes, F.P.J.T.; Wolf, L.B.; Schoe
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(a) Tashiro, T.; Fushiya, S.; Nome,
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Sawada, S.; Nakayama, T.; Esaki, N.
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of Rheum rhaponticum over forty yea
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Glutamic acid derivatives are aiso
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syntheses exist for the functionaii
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4.1.4 Synthesis of Optically Active
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4.1.4.3 Catalytic HydrogeMrion The
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Scheme 4.10 C02Et CO*Et R=Me, Et, P
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stereochemicaî induction at the re
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protected glutamate did not adopt a
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Scheme 4.16 The first synthesis of
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stereoselectivi ty during electroph
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kt, when we repeated the synthesis
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CbzH Scheme 4.2û OH pTsW CbzH Figu
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5.21 5.00 16.63 Figure 4.5: GCMS of
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Glu(y-Me)(OMe)OBO ester 4.73. Howev
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OB0 ester. Moreover, the stereochem
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Table 4.1: Optimilgtion of Methyiat
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Scheme 4.22 M'2aL O 2) 1) LiHMDS, P
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Table 4.2: Optimization of Hydroxyi
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Cb2H 1 OsO,. NMO acetone:H& OH m 2)
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The direct electrophilic azidizatio
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to the mesylate Alûû in 80% yield
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which were not isolated. ESI-MS and
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concentrateci reaction mixhue of 4.
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and during acid hydrolysis. HPLC an
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A general method for the synthesis
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Generai Procedure for Removd of Rot
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Same procedure as in 4.4.1. TU3 (1:
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Same procedure as in 4.4.3. [al% =
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ffom CH2Cl2) 3338,2962,2875, 1732,
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ester -0). 72.4 (OB0 ester w20), 65
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4m4.11 5-Methyl-(~,~-2-[(betl~gIo~)
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= l2JHz, CbzCHHO), 3.87-3.78 (s + r
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1016; HRMS (FAB) calcd for (M + H+)
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7.3&, CHZCH~), 0.78 (s, 3H, OB0 est
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hotu before benzyl brornide (0.21 m
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1 H. J = 10.3Hz (detennined by deco
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378.22; Anal. cdcd for CI9Ha07: C,
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(ça), 164.0 EONH), 143.3 (Cbz==).
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min. The solvent was removed under
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173.8 c=O), 156.3 CONH), 137.6 ( Cb
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mp. 1 16- 1 165°C; [al2'D = -2 1 .
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(3:2 Et0Ac:hexanes) to give 4.99 (1
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Cbz-L-Glu(Z-B,y-dehydro)(OMe)OBO 49
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(CbzQI20), 57.4 (am, 39.8 (yCJS2),
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3.7, 10.7, 14.5Hz. BCHH), 0.76 (S.
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TLC (1:1, EtOAc:Hex), Rc = 0.35; 'H
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1515, 1227, 1048, 1016,909; ESI-MS
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(Cbz=@), 128.5, 128.2, 128.1 (a-=),
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TU3 ( 1 : 1, EtOAc:Hex), Rf = 0.17;
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4-4-46 (2S,4S)-2-My14aminopentanedi
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give 0.020 g (54%) of the monoamrno
Page 259 and 260:
1. (a) Virtanen, A.I.; Berg, A.M. A
Page 261 and 262:
Bory, S.; Dubois, J.; Gaudry, M.; M
Page 263 and 264: (a) Ezquerra, J.; Pedregal, C.; Ymr
Page 265 and 266: (a) Blaskovich, M.A.; Lajoie. G.A.
Page 267 and 268: Rathke, M-W.; Sullivan, D.F. J. Am,
Page 269 and 270: Chapter Five Stereoselective Synthe
Page 271 and 272: of p-methylaspartate 5.1 to glutama
Page 273 and 274: OAc Ac kfN&O@ 5.8 C02Et AC lU&02Et
Page 275 and 276: of 2:7 respectively, both of which
Page 277 and 278: MH). Changing the reaction conditio
Page 279 and 280: Garner's aldehyde 1.53 was also use
Page 281 and 282: Rotected ~-aminoaspartate Sm6 was s
Page 283 and 284: amount of unreacted starting materi
Page 285 and 286: provided crystals of sufficient qua
Page 287 and 288: 5.2.2 Addition of Other AIkylation
Page 289 and 290: Scheme 5-18 We also investigated az
Page 291 and 292: 5.2.5 Discussion of the Stereochist
Page 293 and 294: face) to give rise to the B,3S ster
Page 295 and 296: The synthesis of threo-L-b-substitu
Page 297 and 298: TU3 (1: 1, CHC13:EtOAc, 1 % AcOH) R
Page 299 and 300: 156.0 (ÇONH), 1 36.2 (Cbz*), 128.5
Page 301 and 302: ester COI3), 30.6 (p-cH2), 14.1 (OB
Page 303 and 304: extracted with EtzO (3 x 25 d), the
Page 305 and 306: TU3 (1: 1, EtOAc:Hex), Rr = 0.48; '
Page 307 and 308: 63 MHz) 6 175.9 cd), 156.0 EONH), 1
Page 309 and 310: 175.1 CC-O), 155.8 (CONH), 136.1 (C
Page 311 and 312: 'H-NMR @20, 300 MHz) 6 7.26-7.03 (m
Page 313: 12.7Hz, CbzCHHO), 5.02 (ci, lH, J =
Page 317 and 318: 1. 2. 3. 4. 5. 6. 7. 8. 9. IO. 11.
Page 319 and 320: Eager, R.G. Jr.; Baltimore, B.G.; H
Page 321 and 322: - - Sardina, F.J.; Paz, MM.; Femihd
Page 323 and 324: Chapter Si Solid Phase Synthesis of
Page 325 and 326: eactions such as the Ugi condensati
Page 327 and 328: Dehydroamino acids have also been u
Page 329 and 330: Pyroglutarnate was reduced into the
Page 331 and 332: . - 6.2.1 Synthesis of Resin-Bod BH
Page 333 and 334: " 6.29 NMM, CH& Scheme 6.11 The arn
Page 335 and 336: esin placed hem Figure 6.3: Experim
Page 337 and 338: Figure 6.4: MAS 13c-N..~ (500 MHz)
Page 339 and 340: Table 6.1: Addition of R'M~B~ to 6.
Page 341 and 342: 63 Summ Attachrnent of Ser-OB0 este
Page 343 and 344: (S. 2H, CbzCHzO), 4.57-4.40 (m, 7H,
Page 345 and 346: I C-O), 7 1.9 (OB0 ester GHzO), 61.
Page 347 and 348: insed, altemating with dry DMF (5 x
Page 349 and 350: - MAS 'H NMR (Spin-Echd ms): 8 3.87
Page 351 and 352: 6.4.16 (zs)-2-Pmmo-3-hydroruy-3-met
Page 353 and 354: O.; Gilliarn, CL.; Boisclair, M.D.;
Page 355 and 356: 38. Rakita, P.E.; Silverman, G.S. W
Page 357 and 358: of these important derivatives due
Page 359 and 360: the glutamate dimer. It may also be
Page 361 and 362: Rose, N.G.W.; Blaskovich, M.A.; Won
Page 363 and 364: Appendices
Page 365 and 366:
Table 1, Cryatrl data and .tructuse
Page 367 and 368:
Tabla 3. Bond langths [Al and amglr
Page 369 and 370:
- - - . - Table 5. Eyârogen coordi
Page 371 and 372:
Calculation of Free Energy Dinerenc
Page 373 and 374:
Table 1. Crymtal data and mtructure
Page 375 and 376:
. Tabla 3. Bond lenpths [il and rng
Page 378 and 379:
X-Ray Crystallographic Data for Com
Page 380 and 381:
4 Tabla 2. Atomic coordinates 1 x 1
Page 382 and 383:
2 3 ? able 4. Aniiotsopic dfmplacea
Page 384 and 385:
Calcdation to Determine Resin Loadi
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