Abstract
The Ugi four-component condensation (U-4CC) between arylglyoxals 7 , amines 6 , benzoylformic
acid (4 ) and isocyanides 5 afforded
the expected products 8 which were cyclized
in a 5+1 fashion with ammonium acetate to give 1,N -disubstituted 4-aryl-1,6-dihydro-6-oxo-5-phenylpyrazine-2-carboxamides 9 in good yields. Evidence for the assigned
structures 9 was provided by 13 C
NMR spectra and X-ray analysis of 9a .
Key words
Ugi reaction - cyclizations - heterocycles - isocyanides - pyrazine ring synthesis
References
<A NAME="RT02603SS-1">1 </A>
Barlin GB. In
The Pyrazines
Weissberger A.
Taylor EC.
Wiley-Interscience;
New
York:
1982.
p.49-52
Reviews:
<A NAME="RT02603SS-2A">2a </A>
Marcaccini S.
Torroba T.
Org. Prep. Proc. Int.
1993,
25:
141
<A NAME="RT02603SS-2B">2b </A>
Bossio R.
Marcaccini S.
Pepino R.
Synthesis
1994,
765
<A NAME="RT02603SS-2C">2c </A>
Bossio R.
Marcaccini S.
Pepino R.
Tetrahedron
Lett.
1995,
36:
2325
<A NAME="RT02603SS-2D">2d </A>
Bossio R.
Marcaccini S.
Pepino R.
Torroba T.
J. Org. Chem.
1996,
61:
2202
<A NAME="RT02603SS-2E">2e </A>
Bossio R.
Marcaccini S.
Pepino R.
Torroba T.
J. Chem. Soc., Perkin Trans.
1
1996,
229
<A NAME="RT02603SS-2F">2f </A>
Bossio R.
Fernández Marcos C.
Marcaccini S.
Pepino R.
Tetrahedron
Lett.
1997,
38:
2519
<A NAME="RT02603SS-2G">2g </A>
Bossio R.
Fernández Marcos C.
Marcaccini S.
Pepino R.
Synthesis
1997,
1389
<A NAME="RT02603SS-2H">2h </A>
Bossio R.
Marcaccini S.
Pepino R.
Torroba T.
Heterocycles
1999,
50:
463
<A NAME="RT02603SS-2I">2i </A>
Marcaccini S.
Pepino R.
Polo C.
Pozo MC.
Synthesis
2001,
85
<A NAME="RT02603SS-2J">2j </A>
Marcaccini S.
Pepino R.
Pozo MC.
Tetrahedron
Lett.
2001,
42:
2727
Reviews:
<A NAME="RT02603SS-3A">3a </A>
Ugi I.
Dömling A.
Hörl W.
Endeavour
1994,
18:
115
<A NAME="RT02603SS-3B">3b </A>
Armstrong RW.
Combs AP.
Tempest P.
Brown SD.
Keating TA.
Acc. Chem. Res.
1996,
29:
123
<A NAME="RT02603SS-3C">3c </A>
Ugi I.
Dömling A.
Angew. Chem., Int. Ed.
2000,
39:
3168
<A NAME="RT02603SS-3D">3d </A>
Dömling A.
Comb. Chem. High Throughput Screening
1998,
1:
1
<A NAME="RT02603SS-3E">3e </A>
Bienaymé H.
Hulme C.
Oddon G.
Schmitt P.
Chem.-Eur. J.
2000,
6:
3321
<A NAME="RT02603SS-4A">4a </A>
Janvier P.
Bienaymé H.
Zhu J.
Angew. Chem. Int. Ed.
2002,
41:
4291
<A NAME="RT02603SS-4B">4b </A>
Owens TD.
Semple JE.
Org.
Lett.
2001,
3:
3301
<A NAME="RT02603SS-4C">4c </A>
Tempest P.
Pettus L.
Gore V.
Hulme C.
Tetrahedron Lett.
2003,
44:
1947
<A NAME="RT02603SS-5">5 </A>
Bossio R.
Fernández Marcos C.
Marcaccini S.
Pepino R.
Heterocycles
1997,
45:
1589
Arylglyoxals are useful starting
products in isocyanide-based multi-component reactions:
<A NAME="RT02603SS-6A">6a </A>
Beck B.
Magnin-Lachaux M.
Herdtweck E.
Dömling A.
Org. Lett.
2001,
3:
2875
<A NAME="RT02603SS-6B">6b </A>
Zhang C.
Moran EJ.
Woiwode TF.
Short KM.
Mjalli AMM.
Tetrahedron Lett.
1996,
37:
751
<A NAME="RT02603SS-6C">6c </A>
Sung K.
Wu S.-H.
Chen P.-I.
Tetrahedron
2002,
58:
5599
<A NAME="RT02603SS-7">7 </A>
Gastaldi C.
Princivalle E.
Gazz. Chim. Ital.
1928,
58:
412
<A NAME="RT02603SS-8A">8a </A>
Nishio T.
Tokunaga N.
Kondo M.
Omote Y.
J. Chem.
Soc., Perkin Trans. 1
1988,
2921
<A NAME="RT02603SS-8B">8b </A>
Devys M.
Barbier M.
Kollmann A.
Bousquet J.-F.
Tetrahedron Lett.
1982,
23:
5409
<A NAME="RT02603SS-8C">8c </A>
Nishio T.
J.
Heterocycl. Chem.
1998,
35:
655
<A NAME="RT02603SS-9">9 </A>
Kong YC.
Kim K.
J. Heterocycl. Chem.
1999,
36:
911
<A NAME="RT02603SS-10">10 </A>
Gokel GW.
Widera RP.
Weber WP.
Org. Synth.
1976,
55:
96
<A NAME="RT02603SS-11">11 </A>
Ugi I.
Meyr R.
Lipinsky M.
Bodesheim F.
Rosendahl F.
Org. Synth., Coll. Vol. 5
Wiley;
New
York:
1973.
p.300
<A NAME="RT02603SS-12">12 </A>
Lipp M.
Dallaker F.
Köcker IM.
Monatsh. Chem.
1959,
90:
48
<A NAME="RT02603SS-13">13 </A>
Ugi I.
Meyr R.
Org. Synth.
1961,
41:
101
<A NAME="RT02603SS-14">14 </A>
Riley HA.
Gray AR.
Org.
Synth., Coll. Vol. 2
Wiley;
New
York:
1948.
p.509
<A NAME="RT02603SS-15">15 </A>
Venien F.
Brault A.
Kerfanto M.
C.
R. Acad. Sci. Paris. Ser. C
1968,
266:
1650
<A NAME="RT02603SS-16">16 </A>
Walker N.
Stuart D.
Acta Crystallogr., Sect. A
1983,
39:
158
<A NAME="RT02603SS-17">17 </A>
Altomare A.
Burla MC.
Camalli M.
Cascarano GL.
Giacovazzo C.
Guagliardi A.
Moliterni AG.
Polidori G.
Spagna R.
J.
Appl. Crystallogr.
1999,
32:
115
<A NAME="RT02603SS-18">18 </A>
Sheldrick GM.
SHELXL97: Program for Crystal Structure Refinement
University
of Göttingen;
Germany:
1997.
<A NAME="RT02603SS-19">19 </A>
Crystallographic data have been deposited
at Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2
1EZ, UK and are available from there under the deposition number
CCDC179438.