Chemistry II (Organic)

Transcription

1 Chemistry II (rganic) 1 eteroaromatic Chemistry LECTUE 8 Diazoles & diazines: properties, syntheses & reactivity Alan C. Spivey a.c.spivey@imperial.ac.uk Mar 2012

2 Format & scope of lecture 8 2 Diazoles: Imidazole & pyrazole Structure & properties Synthesis eactivity Diazines: pyrimidines, pyrazines & pyridazines: structure & properties syntheses reactivity

3 Diazoles: Imidazoles & Pyrazoles Importance atural products: 2 histamine (inflammatory) IMIDAZLE 3 C 2 IMIDAZLE histidine (protein constituent) caffeine (tea/coffee stimulant) IMIDAZLE 2 C PYAZLE 4-methylpyrazol-3(5)-carboxylic acid ('fire sponge' marine natural product) Pharmaceuticals: Agrochemicals: S F 3 C 2 PYAZLE CF 3 fipronil (insecticide) IMIDAZLE prochloraz (fungicide)

4 Diazoles Bonding & acid/base properties of pyrazole and imidazole Diazoles can be considered as related to pyrrole but containing an additional in place of one C group: pyrazole 3 imidazole in both cases the new is pyridine-like, i.e. this contributes just 1 electron to the aromatic p-system and has a basic lone pair in the sp 2 orbital in the plane of the ring: For a recent theoretical discussion of pyridine- vs. pyrrole-like s in imidazole see: ichaud rg. Lett. 2011, 972 [DI] Imidazole and pyrazole are both -acidic (pk a s 14.5 & 14.2 respectively; cf. pyrrole 17.5). The basicity of the pyridine-like varies significantly: imidazole is a stronger base than pyridine whereas pyrazole is a weaker base than pyridine: imidazole (pk a 7.0) pyrazole (pk a 2.5) pyridine (pk a 5.2)

5 Imidazole and pyrazole Structure and Properties Imidazole: colourless prisms, mp 88 C; pyrazole: colourless needles, mp 70 C Bond lengths and 1 M chemical shifts as expected for aromatic systems: bond lengths: 1 M: 1.38 Å 1.42 Å cf. ave C-C 1.48 Å 7.1 ppm 1.36 Å 1.33 Å 6.3 ppm 1.37 Å ave C=C 1.34 Å 7.7 ppm 1.31 Å 7.6 ppm 7.1 ppm ave C Å 7.6 ppm 1.37 Å 1.35 Å 1.36 Å 1.35 Å imidazole pyrazole imidazole pyrazole esonance energies: both systems have lower resonance energies than pyrrole (i.e. <90 kjmol -1 ) Electron density: relative to pyrrole, the additional (electronegative) atom decreases the overall electron density on the remaining carbons. The precise distribution is rather uneven: for imidazole: C4 & C5 are electron rich, C2 is electron deficient for pyrazole: C4 is electron rich, C3 & C5 are electron deficient p-electron densities: imidazole pyrazole pyrrole both pyrazole and imidazole are: significantly less reactive towards electrophilic aromatic substitution (S E Ar) than pyrrole (but >benzene) reactive towards nucleophilic aromatic substitution (S Ar) at certain Cs (cf. pyrrole which does not react with nucleophilies)

6 Imidazoles and pyrazoles Syntheses Imidazoles: a-haloketone with amidine: ' ' ' '' ' 2 '' '' 2 '' '' ' 1,2-dicarbonyl & an aldehyde with 3 : ' '' 2x 2 ' + '' 2 ' '' ' Pyrazoles: hydrazine with 1,3-dicarbonyl: ' ' 2 2 ' 2 2 ' 2 ' 1,3-dipolar cycloaddition of diazoalkane with alkyne: ' '' ' '' # ' '' ' ''

7 Imidazoles and pyrazoles eactivity Electrophilic substitution: via addition-elimination (S E Ar): reactivity: reactive towards many electrophiles (E + ); >benzene but <pyrrole, furan & thiophene regioselectivity: substitution at electron rich carbons predominate (cf. electronic distribution): imidazole: C4 > C5 (for systems; if then C4 and C5 are identical) pyrazole: C4 less reactive than imidazole imidazole E 4 pyrazole E 4 E 5 e.g. nitration: (E + = 2+ ) imidazole: ) 3 2) a e.g. chlorination: (E + = + ) pyrazole: 2, Ac 4 B. electron donating substituents enhance reactivity towards electrophiles

8 Imidazoles and pyrazoles eactivity cont. ucleophilic substitution: via addition-elimination (S Ar) reactivity: reactive towards good nucleophilies (u - ) provided leaving group is situated at appropriate carbon regioselectivity: substitution of leaving groups (e.g., Br, 2 ) at electron deficient centres possible (cf. electronic distribution): imidazole: C2 relatively reactive centre pyrazole: C5 ~ C3 neither centre very reactive imidazole 2 pyrazole LG (difficult) u u LG 5 3 LG u e.g. displacement of Br by amine: (u - = 2 -, LG = Br) imidazole: Br 200 C 2 B. electron withrawing substituents enhance reactivity towards nucleophiles

9 Imidazoles and pyrazoles eactivity cont. tallation: (imidazole pk a = 14.5; pyrazole pk a = 14.2) deprotonation by strong bases more facile than for pyrrole (pk a = 17.5) or indole (pk a = 16.2):

10 Diazines: Pyrimidines, Pyridazines & Pyrazines Importance atural products: Pharmaceuticals: 2 PYIMIDIE PYIMIDIE PYAZIE 2 C Et S orotic acid thiamine - vitamin B1 aspergillic acid (biosynthetic intermediate (essential vitamin) (fungal antibiotic) for natural pyrimidines) Agrochemicals: PYIMIDIE 2 C S Bu t PYIDIZIE t Bu PYIDIZIE SEt P PYAZIE bensulfuronmethyl (herbicide) pyridaben (herbicide) maleic hydrazide (plant growth inhibitor) thionazin (soil insecticide)

11 Diazines Bonding, Structure & Properties Diazines can be considered as related to pyridine but containing an additional in place of one C group: pyrimidine 1 3 pyrazine 4 1 pyridazine in all cases the new is pyridine-like, i.e. this contributes just 1 electron to the aromatic p-system and has a basic lone pair in the sp 2 orbital in the plane of the ring: pyrimidine pyrazine pyridazine All three diazines are significantly less basic than pyridine: pyrimidine (pk a 1.3) pyrazine (pk a 0.4) pyridazine (pk a 2.3)

12 Diazines Structure and Properties Pyrimidine: colourless prisms, mp 22 C Pyridazine: colourless liquid, bp 208 C Pyrazine: colourless prisms, mp 57 C Bond lengths and 1 M chemical shifts as expected for aromatic systems: bond lengths: 1.40 Å 1.35 Å 1.34 Å pyrimidine 1.37 Å 1.39 Å 1.39 Å 1.34 Å 1.34 Å 1.33 Å pyrazine pyridazine cf. ave C-C 1.48 Å ave C=C 1.34 Å ave C Å 1 M: 7.4 ppm 8.8 ppm 9.3 ppm pyrimidine 7.5 ppm 9.2 ppm 8.6 ppm pyrazine pyridazine esonance energies: all three systems have lower resonance energies than pyridine (117 kjmol -1 ) susceible to nucleophilic addition reactions Electron density: all three systems are highly electron deficient (cf. ~pyridine) unreactive towards electrophiic substitution (S E Ar) reactive towards nucleophilic substitution (S Ar)

13 Diazines Syntheses Pyrimidines: Pinner: 1,3-dicarbonyl with amidine Et Et 2 Et Et 2 Et Pyrazines: dimerisation of a-aminoketone/aldehyde then aerial oxidation: C , Pd/C 2 2 air Pyridazines: Paal-Knorr : 1,4-dicarbonyl with hydrazine B. hydroxyl 'leaving group' in 1,4-dicarbonyl obviates oxidation

14 Diazines eactivity Electrophilic addition at : formation of -oxides as for pyridine; these derivatives are more susceible to S Ar (and S E Ar) than the parent diazines: Electrophilic substitution: via addition-elimination (S E Ar) all diazines are highly electron deficient very unreactive towards S E Ar electron donating substituents and/or -oxides (see above) required to allow reaction even at C5 of pyrimidine: 3x electron releasing i.e. 'activating' groups c. 3 /Ac C 2 [85%] B. no reaction on pyrimidine itself regioselectivity: via most stable Wheland intermediate

15 Diazines eactivity ucleophilic substitution: via addition-elimination (S Ar) all diazines are highly electron deficient very reactive towards S Ar (>pyridines) all halodiazines exce 5-halopyrimidines react readily with nucleophilies: tallation: all diazines can be metalated ortho to by LiTMP (pyrimidine at C4 not C2): pyrazine Li 2 Li I 2 I [44%] pyrazine--oxide Bu Bu Li Bu Li Bu I 2 Bu I Bu [73%]