Abstract
A convenient method for the synthesis of a novel series of eighteen non-condensed
5,5-bicycles, specifically 2-[3-alkyl(phenyl)-5-hydroxy-5-trifluoromethyl-4,5-dihydro-1H -pyrazol-1-yl]-4-phenyl-5-alkylthiazoles and -4,5,6,7-tetrahydrobenzothiazoles 3a -i from the reaction of 3-alkyl(phenyl)-5-hydroxy-5-trifluoromethyl-4,5-dihydro-1H -1-pyrazolethiocarboxyamide (1 ) with 2-bromoacetophenone, 2-bromopropiophenone and 2-bromocyclohexanone (2 ), is reported. The dehydration of compounds 3a -i with a mixture of concentrated sulfuric acid-acetic acid (1:10 v/v) led to the corresponding
2-[3-alky(phenyl)-5-trifluoromethyl-1H -pyrazol-1-yl]-4-phenyl-5-alkylthiazoles and respective 4,5,6,7-tetrahydrobenzothiazoles
4a -i in good yield.
Key words
thiazoles - benzothiazoles - fluorine - heterocycles - pyrazoles - cyclizations
References
<A NAME="RM06201SS-1">1 </A>
Katritzky AR.
Rees CW.
Scriven EFV.
Comprehensive Heterocyclic Chemistry II
Vol. 3:
Elsevier Science;
NY:
1996.
<A NAME="RM06201SS-2">2 </A>
Lednicer D.
Mitscher LA.
Organic Chemistry of Drugs Synthesis
Vol. 1-3:
Wiley Interscience;
New York:
1977.
<A NAME="RM06201SS-3">3 </A>
De Arriba AF.
Gómez-Casajús LA.
Cavalcanti F.
Almansa C.
García-Rafanell J.
Forn J.
Eur. J. Pharmacol.
1996,
318:
341
<A NAME="RM06201SS-4">4 </A>
De Arriba AF.
Gómez-Casajús LA.
Cavalcanti F.
Almansa C.
García-Rafanell J.
Forn J.
J. Med. Chem.
1997,
40:
547
<A NAME="RM06201SS-5">5 </A>
Harper RW.
Jackson WT.
Froelich LL.
Boyd RJ.
Aldridge TE.
Herron DK.
J. Med. Chem.
1994,
37:
2411
<A NAME="RM06201SS-6">6 </A>
Ishii S,
Yagi K,
Umehara T,
Kudo M,
Nawamaki T, and
Watanabe S. inventors; Jpn. Kokai Tokkyo Koho JP 02, 129.
171 ; Chem. Abstr.
1990 ,
113 , 172014a
<A NAME="RM06201SS-7">7 </A>
Buntain IG,
Hatton LR,
Hawkins DW,
Pearson CJ, and
Roberts DA. inventors; Eur. Pat. Appl. EP 295 117.
; Chem. Abstr.
1990 , 112 , 35845n
<A NAME="RM06201SS-8">8 </A>
Nenajdenko VG.
Sanin AV.
Balenkova ES.
Molecules
1997,
2:
186
<A NAME="RM06201SS-9">9 </A>
Welch JT.
Tetrahedron
1987,
43:
3123
<A NAME="RM06201SS-10">10 </A>
Denisova AB.
Glukhareva TV.
Mokrushin VS.
Bakulev VA.
Chem. Heterocycl. Compd. (N. Y.)
1999,
35:
123
<A NAME="RM06201SS-11">11 </A>
Metzger JV.
Comp. Heterocycl. Chem.
1984,
6:
294
<A NAME="RM06201SS-12">12 </A>
Sing SP.
Kumar D.
Kapoor JK.
J. Chem. Research (S)
1993,
163
<A NAME="RM06201SS-13">13 </A>
Peet NP.
Sunder S.
Barbuch RJ.
Whalon MR.
J. Heterocycl. Chem.
1988,
25:
543
<A NAME="RM06201SS-14">14 </A>
Singh SP.
Kumar D.
Jones BG.
Threadgill MD.
J. Fluorine Chem.
1999,
94:
1999
<A NAME="RM06201SS-15">15 </A>
Rezessy B.
Zubovics Z.
Kovács J.
Tóth G.
Tetrahedron
1999,
55:
5909
<A NAME="RM06201SS-16">16 </A>
Saloutina LV.
Zapevalov A.
Kodess MI.
Saloutin VI.
Aleksandrov GG.
Chupakhin ON.
J. Fluorine Chem.
2000,
104:
155
<A NAME="RM06201SS-17">17 </A>
Martins MAP.
Flores AFC.
Freitag RA.
Zanatta N.
J. Heterocycl. Chem.
1995,
32:
731
<A NAME="RM06201SS-18">18 </A>
Zoch AN.
Clar G.
Zanatta N.
Bonacorso HG.
Martins MAP.
J. Heterocycl. Chem.
1995,
32:
739
<A NAME="RM06201SS-19">19 </A>
Martins MAP.
Flores AFC.
Freitag R.
Zanatta N.
J. Heterocycl. Chem.
1996,
33:
1223
<A NAME="RM06201SS-20">20 </A>
Martins MAP.
Siqueira GM.
Bastos GP.
Bonacorso HG.
Zanatta N.
J. Heterocycl. Chem.
1996,
33:
1619
<A NAME="RM06201SS-21">21 </A>
Braibante MEF.
Clar G.
Martins MAP.
J. Heterocycl. Chem.
1993,
30:
1159
<A NAME="RM06201SS-22">22 </A>
Martins MAP.
Freitag R.
Zanatta N.
Synthesis
1995,
1491
<A NAME="RM06201SS-23">23 </A>
Pacholski IL.
Blanco I.
Zanatta N.
Martins MAP.
J. Braz. Chem. Soc.
1991,
2:
118 ; Chem. Abstr. 1994 , 120 , 323443n
<A NAME="RM06201SS-24">24 </A>
Madruga CC.
Clerici E.
Martins MAP.
Zanatta N.
J. Heterocycl. Chem.
1995,
32:
735
<A NAME="RM06201SS-25">25 </A>
Zanatta N.
Cortelini MFM.
Carpes MJS.
Bonacorso HG.
Martins MAP.
J. Heterocycl. Chem.
1997,
34:
509
<A NAME="RM06201SS-26">26 </A>
Bonacorso HG.
Bittencourt SRT.
Wastowski AD.
Wentz AP.
Zanatta N.
Martins MAP.
Tetrahedron Lett.
1996,
37:
9155
<A NAME="RM06201SS-27">27 </A>
Bonacorso HG.
Bittencourt SRT.
Lourega RV.
Flores AFC.
Zanatta N.
Martins MAP.
Synthesis
2000,
1431
<A NAME="RM06201SS-28">28 </A>
Bonacorso HG.
Oliveira MR.
Wentz AP.
Wastowski AD.
Oliveira AB.
Höerner M.
Zanatta N.
Martins MAP.
Tetrahedron
1999,
55:
345
<A NAME="RM06201SS-29">29 </A>
Bonacorso HG.
Wastowski AD.
Zanatta N.
Martins MAP.
Naue JA.
J. Fluorine Chem.
1998,
92:
23