Abstract
Maleimidoalkanoic acids and their activated derivatives, such as their N -hydroxysuccinimide esters, are important, though expensive, linkers for the conjugation
of biomolecules. During our synthesis of UCS1025A, we have developed a chromatography-free
preparation of 4-maleimidobutyric acid on a one-mole scale.
Key words
imides - condensations - maleic anhydride - aminobutanoic acid - cross-linking reagents
References
<A NAME="RE19307SS-1">1 </A>
Rich DH.
Gesellchen PD.
Tong A.
Cheung A.
Buckner CK.
J. Med. Chem.
1975,
18:
1004
<A NAME="RE19307SS-2A">2a </A>
Stuhlmann F.
Jäschke A.
J. Am. Chem. Soc.
2002,
124:
3238
<A NAME="RE19307SS-2B">2b </A>
Herrmann A.
Mihov G.
Vandermeulen GWM.
Klok H.-A.
Müllen K.
Tetrahedron
2003,
59:
3925
<A NAME="RE19307SS-2C">2c </A>
Bennes RM.
Philp D.
Org. Lett.
2006,
8:
3651
<A NAME="RE19307SS-2D">2d </A>
de Araújo AD.
Palomo JM.
Cramer J.
Seitz O.
Alexandrov K.
Waldmann H.
Chem. Eur. J.
2006,
12:
6095
<A NAME="RE19307SS-2E">2e </A>
Meyer-Losic F.
Quinonero J.
Dubois V.
Alluis B.
Dechambre M.
Michel M.
Cailler F.
Fernandez A.-M.
Trouet A.
Kearsey J.
J. Med. Chem.
2006,
49:
6908
<A NAME="RE19307SS-3">3 </A>
Lambert TH.
Danishefsky SJ.
J. Am. Chem. Soc.
2006,
128:
426
<A NAME="RE19307SS-4">4 </A>
Hoye TR.
Dvornikovs V.
J. Am. Chem. Soc.
2006,
128:
2550
<A NAME="RE19307SS-5A">5a </A>
Nakai R.
Ogawa H.
Asai A.
Ando K.
Agatsuma T.
Matsumiya S.
Akinaga S.
Yamashita Y.
Mizukami T.
J. Antibiot.
2000,
53:
294
<A NAME="RE19307SS-5B">5b </A>
Agatsuma T.
Akama T.
Nara S.
Matsumiya S.
Nakai R.
Ogawa H.
Otaki S.
Ikeda S.-i.
Saitoh Y.
Kanda Y.
Org. Lett.
2002,
4:
4387
<A NAME="RE19307SS-5C">5c </A>
Nakai R.
Ishida H.
Asai A.
Ogawa H.
Yamamoto Y.
Kawasaki H.
Akinaga S.
Mizukami T.
Yamashita Y.
Chem. Biol.
2006,
13:
183
<A NAME="RE19307SS-6A">6a </A>
de Figueiredo RM.
Fröhlich R.
Christmann M.
Angew. Chem. Int. Ed.
2007,
46:
2883
<A NAME="RE19307SS-6B">6b </A>
de Figueiredo RM.
Voith M.
Fröhlich R.
Christmann M.
Synlett
2007,
391
<A NAME="RE19307SS-7A">7a </A>
Mantovani G.
Lecolley F.
Tao L.
Haddleton DM.
Clerx J.
Cornelissen JJLM.
Velonia K.
J. Am. Chem. Soc.
2005,
127:
2966
<A NAME="RE19307SS-7B">7b </A>
Lavis LD.
Chao T.
Raines RT.
ACS Chem. Biol.
2006,
1:
252
<A NAME="RE19307SS-8">8 </A>
CCDC 651593 contains the supplementary crystallographic data for this paper. These
data can be obtained free of charge at www.ccdc.cam.ac.uk/conts/retrieving.html [or
from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ,
UK, fax: +44(1223)336033, E-mail: deposit@ccdc.cam.ac.uk.